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140-90-9

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  • Sodium ethylxanthogenate CAS 140-90-9 Sodium O-ethyl dithiocarbonate CAS no 140-90-9 Sodium ethyl xanthate

    Cas No: 140-90-9

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140-90-9 Usage

Chemical Properties

Sodium ethylxanthogenate is a light yellow powder (granular) with a pungent odor, soluble in water, alcohol, etc., and can form insoluble compounds with metal ions such as cobalt, copper, and nickel.

Uses

Sodium ethylxanthogenate can be widely used in the preferential flotation or complex non-ferrous metal sulfide ores, and can also be used with vulcanizing agents for the flotation of copper and lead oxide ores.

Flammability and Explosibility

Highlyflammable

Check Digit Verification of cas no

The CAS Registry Mumber 140-90-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 140-90:
(5*1)+(4*4)+(3*0)+(2*9)+(1*0)=39
39 % 10 = 9
So 140-90-9 is a valid CAS Registry Number.
InChI:InChI=1/C3H6OS2.Na/c1-2-4-3(5)6;/h2H2,1H3,(H,5,6);/q;+1/p-1

140-90-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium ethylxanthogenate

1.2 Other means of identification

Product number -
Other names Ethylxanthic Acid Sodium Salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:140-90-9 SDS

140-90-9Synthetic route

carbon disulfide
75-15-0

carbon disulfide

ethanol
64-17-5

ethanol

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium hydroxide In tetrahydrofuran at 10 - 20℃; for 2h; Temperature;97.4%
With sodium hydroxide In water for 4h;80.4%
With sodium for 6h; Heating;63%
sodium ethanolate
141-52-6

sodium ethanolate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With carbon disulfide
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

A

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

B

C8H15NOS4
327989-09-3

C8H15NOS4

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

sodium dibenzyldithiocarbamate
55310-46-8

sodium dibenzyldithiocarbamate

A

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

B

C18H19NOS4

C18H19NOS4

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

C8H15NOS4
327989-09-3

C8H15NOS4

A

disulfiram
97-77-8

disulfiram

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
sodium dibenzyldithiocarbamate
55310-46-8

sodium dibenzyldithiocarbamate

C18H19NOS4

C18H19NOS4

A

bis(dibenzylthiocarbamoyl)disulfide
10591-85-2

bis(dibenzylthiocarbamoyl)disulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
ethanol
64-17-5

ethanol

CS2

CS2

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium hydroxide
sodium ethanolate
141-52-6

sodium ethanolate

CS2

CS2

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With ethanol
With ethanol
carbon disulfide
75-15-0

carbon disulfide

sodium ethanolate
141-52-6

sodium ethanolate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
at 0 - 20℃;
catalyst
ethanol
64-17-5

ethanol

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium hydrogen sulfide

sodium hydrogen sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
In water ambient temp., 5 h;
In water ambient temp., 5 h;
ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium hydrogen sulfide

sodium hydrogen sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C

sodium ethyl carbonate
17201-44-4

sodium ethyl carbonate

D

sodium thiosulfate

sodium thiosulfate

Conditions
ConditionsYield
In ethanol 30 min;
In ethanol 30 min;
ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium sulfide

sodium sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C

sodium ethyl carbonate
17201-44-4

sodium ethyl carbonate

D

sodium thiosulfate

sodium thiosulfate

Conditions
ConditionsYield
In ethanol 30 min;
In ethanol 30 min;
2-fluro-4-iodoaniline
29632-74-4

2-fluro-4-iodoaniline

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

6-iodobenzo[d]thiazole-2-thiol
54420-94-9

6-iodobenzo[d]thiazole-2-thiol

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 95℃; for 5h;100%
2,15-bis(chloromethyl)-4,7,10,13-tetraoxahexadeca-1,15-diene
1401454-94-1

2,15-bis(chloromethyl)-4,7,10,13-tetraoxahexadeca-1,15-diene

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S,S'-2,15-dimethylene-4,7,10,13-tetraoxahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate
1401454-99-6

S,S'-2,15-dimethylene-4,7,10,13-tetraoxahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate

Conditions
ConditionsYield
In ethanol at 20 - 35℃; Inert atmosphere;98%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

S-(ethoxycarbonyl) O-ethyl dithiocarbonate
3278-35-1

S-(ethoxycarbonyl) O-ethyl dithiocarbonate

Conditions
ConditionsYield
With cetyltrimethylammonim bromide In N,N-dimethyl-aniline at 10 - 25℃; for 4h;97.1%
2,15-bis(chloromethyl)-7,10-dioxa-4,13-dithiahexadeca-1,15-diene
1326703-36-9

2,15-bis(chloromethyl)-7,10-dioxa-4,13-dithiahexadeca-1,15-diene

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S,S'-2,15-dimethylene-7,10-dioxa-4,13-dithiahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate
1401455-02-4

S,S'-2,15-dimethylene-7,10-dioxa-4,13-dithiahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate

Conditions
ConditionsYield
In ethanol at 20 - 35℃; Inert atmosphere;97%
2-chloro-4-fluoroaniline
2106-02-7

2-chloro-4-fluoroaniline

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

6-fluoro-1,3-benzothiazole-2(3H)-thione

6-fluoro-1,3-benzothiazole-2(3H)-thione

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 100℃; for 4h;96%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

bis(dichlorostibino)methane
32278-97-0

bis(dichlorostibino)methane

{Sb(S2COC2H5)2}2CH2

{Sb(S2COC2H5)2}2CH2

Conditions
ConditionsYield
In methanol byproducts: NaCl; addition of a solution of 6.00 mmol of NaS2COEt in 20 ml CH3OH drop by drop to a solution of 1.50 mmol of (Cl2Sb)2CH2 (1 hour) and stirring at 25°C, 3 - 5 hours;; filtration, washing with CH3OH and drying; elem. anal.;;96%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

S-allyl O-ethyl dithiocarbonate
7124-50-7

S-allyl O-ethyl dithiocarbonate

Conditions
ConditionsYield
With cetyltrimethylammonim bromide at 25℃; for 6.5h;95.3%
di-n-propylammonium hydrogen sulphate
908126-51-2

di-n-propylammonium hydrogen sulphate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S-ethyl N,N-di-n-propylthiocarbamate
759-94-4

S-ethyl N,N-di-n-propylthiocarbamate

Conditions
ConditionsYield
Stage #1: di-n-propylammonium hydrogen sulphate; sodium O-ethyl dithiocarbonate With dihydrogen peroxide In water at 40℃; for 1h; Green chemistry;
Stage #2: With sulfuric acid In water at 70℃; for 1h; pH=7; Green chemistry;
94%
μ-oxo-bis{bromotrimethyl-λ5-stibane}
10369-54-7

μ-oxo-bis{bromotrimethyl-λ5-stibane}

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

{(CH3)3SbS2COC2H5}2O
140405-09-0

{(CH3)3SbS2COC2H5}2O

Conditions
ConditionsYield
In dichloromethane byproducts: NaBr; addition of a twofold excess of NaS2COEt to a suspension of 2 mmol of (Me3SbBr)2O in 10 ml CH2Cl2 at -30°C, stirring (2 hours), filtration and evaporation;; recrystallization from diethyl ether; elem. anal.;;93%
tetraethylammonium chloropentacarbonyltungstate
14780-97-3

tetraethylammonium chloropentacarbonyltungstate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

(CH3CH2)4N(1+)*W(CO)4(SSCOCH2CH3)(1-)=((CH3CH2)4N)[W(CO)4(SSCOCH2CH3)]
922713-51-7

(CH3CH2)4N(1+)*W(CO)4(SSCOCH2CH3)(1-)=((CH3CH2)4N)[W(CO)4(SSCOCH2CH3)]

Conditions
ConditionsYield
In acetonitrile byproducts: NaCl, CO; under N2; Schlenk technique; mixt. of W compd. and Na salt in CH3CN refluxed for 2 h; evapn. under vac., residue dissolved in THF/acetone (10/1), filtration through silica/celite, filtrate evapd., residue washed with Et2O; elem. anal.;93%
3-(2-methylphenyl)prop-2-en-1-al
93614-78-9, 4549-82-0

3-(2-methylphenyl)prop-2-en-1-al

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

cyclohexylamine
108-91-8

cyclohexylamine

3-cyclohexyl-4-hydroxy-6-(2-methylphenyl)-1,3-thiazinane-2-thione

3-cyclohexyl-4-hydroxy-6-(2-methylphenyl)-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In chloroform at 61℃; for 1.83333h;92.7%
diisopropylammonium hydrogen sulphate
65087-26-5

diisopropylammonium hydrogen sulphate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

diisopropyl-thiocarbamic acid S-ethyl ester
63644-60-0

diisopropyl-thiocarbamic acid S-ethyl ester

Conditions
ConditionsYield
Stage #1: diisopropylammonium hydrogen sulphate; sodium O-ethyl dithiocarbonate With dihydrogen peroxide In water at 45℃; for 1.5h; Green chemistry;
Stage #2: With sulfuric acid In water at 75℃; for 2.2h; pH=7; Green chemistry;
92%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

methylmercury(II) chloride
115-09-3

methylmercury(II) chloride

CH3Hg(S2COCH2CH3)
104855-65-4

CH3Hg(S2COCH2CH3)

Conditions
ConditionsYield
In dichloromethane MeHgCl dissolved in CH2Cl2 was treated with ligand, stirred at room temp. for 1 h; filtered, evapd. in open air, redissolved in CH2Cl2, filtered, covered with petroleum ether, crystd. in reflrigerator, filtered, dried in vacuo;elem. anal.;91.7%
hexan-1-amine
111-26-2

hexan-1-amine

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

3-(4-methylphenyl)acrylaldehyde
1504-75-2

3-(4-methylphenyl)acrylaldehyde

3-n-hexyl-4-hydroxy-6-(4-methylphenyl)-1,3-thiazinane-2-thione

3-n-hexyl-4-hydroxy-6-(4-methylphenyl)-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In methanol at 65℃; for 1.08333h;91.7%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

4-methoxy-aniline
104-94-9

4-methoxy-aniline

jasminaldehyde
122-40-7

jasminaldehyde

5-pentyl-3-(4-methoxyphenyl)-4-hydroxy-6-phenyl-1,3-thiazinane-2-thione

5-pentyl-3-(4-methoxyphenyl)-4-hydroxy-6-phenyl-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In dichloromethane at 25℃; for 1.66667h;90.7%
((Pd(μ-I)((CH2)2S(O)Me))2)

((Pd(μ-I)((CH2)2S(O)Me))2)

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Pd{(CH2)2(SO)(CH3)}(S2COC2H5)

Pd{(CH2)2(SO)(CH3)}(S2COC2H5)

Conditions
ConditionsYield
In dichloromethane Addn. of org. compd. to suspn. of Pd-complex (CH2Cl2) using n-Bu4NI as phase transfer catalyst and stirring. The yellow solid is dissolved within 6 min.; Washing of ppt. with H2O (3 times), removal of solvent, recrystn. of residue from n-hexane/CH2Cl2, elem. anal.;90%
In dichloromethane Addn. of org. compd. to suspn. of Pd-complex (CH2Cl2) and stirring. The yellow solid is dissolved within 15 min.;79%
silver tetrafluoroborate
14104-20-2

silver tetrafluoroborate

bis(η5-cyclopentadinyl)dihydridomolybdenum

bis(η5-cyclopentadinyl)dihydridomolybdenum

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

[((C5H5)2MoH2)2AgS2COC2H5]

[((C5H5)2MoH2)2AgS2COC2H5]

Conditions
ConditionsYield
In acetone (N2); NaS2COEt/acetone added at -30°C to soln. of Mo complex andAgBF4 in acetone; ppt. isolated, washed (Et2O), chromd. (SiO2, CH2Cl2/acetone), recrystd.(acetone); elem. anal.;90%
dioxomolybdenum(VI) dibromide bis(dimethylsulfoxide)

dioxomolybdenum(VI) dibromide bis(dimethylsulfoxide)

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

MoO2Br(O-ethyl dithiocarbonate)(dimethylsulfoxide)

MoO2Br(O-ethyl dithiocarbonate)(dimethylsulfoxide)

Conditions
ConditionsYield
In dichloromethane byproducts: NaBr, Me2SO; suspn. of Na-compound in CH2Cl2 added to soln. of Mo-compound in CH2Cl2 in 1:1 molar ratio with constant stirring; stirred for 3 h; filtered; washed with CH2Cl2; excess solvent removed; dried in vacuo; washed repeatedly with dried benzene; elem. anal.;89%
{C5H5Ni(P(C4H9-n)3)2}Cl

{C5H5Ni(P(C4H9-n)3)2}Cl

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C5H5Ni(P(C4H9-n)3)SC(S)OC2H5
52247-33-3

C5H5Ni(P(C4H9-n)3)SC(S)OC2H5

Conditions
ConditionsYield
In water room temp.; with excess of NaSC(S)OC2H5; extn. of the brown ppt. with ether or benzene; drying, evapn. in vac.; recrystn. from benzene or benzene/hexane;88%
In water
iron(III) chloride hexahydrate

iron(III) chloride hexahydrate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

1,2-bis-(diphenylphosphino)ethane
1663-45-2

1,2-bis-(diphenylphosphino)ethane

[Fe(diphenylphosphinoethane)(ethyl xanthate)2]
1180915-75-6

[Fe(diphenylphosphinoethane)(ethyl xanthate)2]

Conditions
ConditionsYield
With ascorbic acid In ethanol; dichloromethane; water soln. of ascorbic acid in EtOH/H2O (9:1 v/v) was added with stirring to soln. of FeCl3*6H2O in EtOH, heated to 70°C, soln. of dppe in CH2Cl2 was added, stirred for 15 min, cooled to r.t., soln. of Na-xanthate in EtOH was added; filtered off, washed with water, EtOH, Et2O, crystd. from CHCl3/Et2O (4:1), elem. anal.;88%
With HCl; NH2OH*HCl In ethanol; dichloromethane byproducts: NaCl; soln. of NH2OH*HCl in EtOH was added to soln. of FeCl3*6H2O and aq. HCl in EtOH, warmed at 60-70°C for 10 min, filtered, soln. of dppe in CH2Cl2 was added to filtrate, stirred for 15-20 min, filtered, soln. of Na-xanthate in EtOH was added; filtered, washed with water, 90% EtOH, Et2O, crystd. form CH2Cl2/Et2O (6:1), elem. anal.;
carbon disulfide
75-15-0

carbon disulfide

ethanol
64-17-5

ethanol

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium hydroxide In tetrahydrofuran at 10 - 20℃; for 2h; Temperature;97.4%
With sodium hydroxide In water for 4h;80.4%
With sodium for 6h; Heating;63%
sodium ethanolate
141-52-6

sodium ethanolate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With carbon disulfide
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

A

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

B

C8H15NOS4
327989-09-3

C8H15NOS4

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

sodium dibenzyldithiocarbamate
55310-46-8

sodium dibenzyldithiocarbamate

A

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

B

C18H19NOS4

C18H19NOS4

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
sodium N,N-diethyldithiocarbamate
148-18-5

sodium N,N-diethyldithiocarbamate

C8H15NOS4
327989-09-3

C8H15NOS4

A

disulfiram
97-77-8

disulfiram

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
sodium dibenzyldithiocarbamate
55310-46-8

sodium dibenzyldithiocarbamate

C18H19NOS4

C18H19NOS4

A

bis(dibenzylthiocarbamoyl)disulfide
10591-85-2

bis(dibenzylthiocarbamoyl)disulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium nitrate; C8MoN8(3-)*3Na(1+) In water; acetone at 25℃; Equilibrium constant; μ 0.2 mol/l;
ethanol
64-17-5

ethanol

CS2

CS2

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With sodium hydroxide
sodium ethanolate
141-52-6

sodium ethanolate

CS2

CS2

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
With ethanol
With ethanol
carbon disulfide
75-15-0

carbon disulfide

sodium ethanolate
141-52-6

sodium ethanolate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
at 0 - 20℃;
catalyst
ethanol
64-17-5

ethanol

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium hydrogen sulfide

sodium hydrogen sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Conditions
ConditionsYield
In water ambient temp., 5 h;
In water ambient temp., 5 h;
ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium hydrogen sulfide

sodium hydrogen sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C

sodium ethyl carbonate
17201-44-4

sodium ethyl carbonate

D

sodium thiosulfate

sodium thiosulfate

Conditions
ConditionsYield
In ethanol 30 min;
In ethanol 30 min;
ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

sodium trithiocarbonate
534-18-9

sodium trithiocarbonate

A

sodium sulfide

sodium sulfide

B

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

C

sodium ethyl carbonate
17201-44-4

sodium ethyl carbonate

D

sodium thiosulfate

sodium thiosulfate

Conditions
ConditionsYield
In ethanol 30 min;
In ethanol 30 min;
2-fluro-4-iodoaniline
29632-74-4

2-fluro-4-iodoaniline

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

6-iodobenzo[d]thiazole-2-thiol
54420-94-9

6-iodobenzo[d]thiazole-2-thiol

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 95℃; for 5h;100%
2,15-bis(chloromethyl)-4,7,10,13-tetraoxahexadeca-1,15-diene
1401454-94-1

2,15-bis(chloromethyl)-4,7,10,13-tetraoxahexadeca-1,15-diene

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S,S'-2,15-dimethylene-4,7,10,13-tetraoxahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate
1401454-99-6

S,S'-2,15-dimethylene-4,7,10,13-tetraoxahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate

Conditions
ConditionsYield
In ethanol at 20 - 35℃; Inert atmosphere;98%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

S-(ethoxycarbonyl) O-ethyl dithiocarbonate
3278-35-1

S-(ethoxycarbonyl) O-ethyl dithiocarbonate

Conditions
ConditionsYield
With cetyltrimethylammonim bromide In N,N-dimethyl-aniline at 10 - 25℃; for 4h;97.1%
2,15-bis(chloromethyl)-7,10-dioxa-4,13-dithiahexadeca-1,15-diene
1326703-36-9

2,15-bis(chloromethyl)-7,10-dioxa-4,13-dithiahexadeca-1,15-diene

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S,S'-2,15-dimethylene-7,10-dioxa-4,13-dithiahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate
1401455-02-4

S,S'-2,15-dimethylene-7,10-dioxa-4,13-dithiahexadecane-1,16-diyl O,O'-diethyl dicarbonodithioate

Conditions
ConditionsYield
In ethanol at 20 - 35℃; Inert atmosphere;97%
2-chloro-4-fluoroaniline
2106-02-7

2-chloro-4-fluoroaniline

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

6-fluoro-1,3-benzothiazole-2(3H)-thione

6-fluoro-1,3-benzothiazole-2(3H)-thione

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 100℃; for 4h;96%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

bis(dichlorostibino)methane
32278-97-0

bis(dichlorostibino)methane

{Sb(S2COC2H5)2}2CH2

{Sb(S2COC2H5)2}2CH2

Conditions
ConditionsYield
In methanol byproducts: NaCl; addition of a solution of 6.00 mmol of NaS2COEt in 20 ml CH3OH drop by drop to a solution of 1.50 mmol of (Cl2Sb)2CH2 (1 hour) and stirring at 25°C, 3 - 5 hours;; filtration, washing with CH3OH and drying; elem. anal.;;96%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

3-chloroprop-1-ene
107-05-1

3-chloroprop-1-ene

S-allyl O-ethyl dithiocarbonate
7124-50-7

S-allyl O-ethyl dithiocarbonate

Conditions
ConditionsYield
With cetyltrimethylammonim bromide at 25℃; for 6.5h;95.3%
di-n-propylammonium hydrogen sulphate
908126-51-2

di-n-propylammonium hydrogen sulphate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

S-ethyl N,N-di-n-propylthiocarbamate
759-94-4

S-ethyl N,N-di-n-propylthiocarbamate

Conditions
ConditionsYield
Stage #1: di-n-propylammonium hydrogen sulphate; sodium O-ethyl dithiocarbonate With dihydrogen peroxide In water at 40℃; for 1h; Green chemistry;
Stage #2: With sulfuric acid In water at 70℃; for 1h; pH=7; Green chemistry;
94%
μ-oxo-bis{bromotrimethyl-λ5-stibane}
10369-54-7

μ-oxo-bis{bromotrimethyl-λ5-stibane}

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

{(CH3)3SbS2COC2H5}2O
140405-09-0

{(CH3)3SbS2COC2H5}2O

Conditions
ConditionsYield
In dichloromethane byproducts: NaBr; addition of a twofold excess of NaS2COEt to a suspension of 2 mmol of (Me3SbBr)2O in 10 ml CH2Cl2 at -30°C, stirring (2 hours), filtration and evaporation;; recrystallization from diethyl ether; elem. anal.;;93%
tetraethylammonium chloropentacarbonyltungstate
14780-97-3

tetraethylammonium chloropentacarbonyltungstate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

(CH3CH2)4N(1+)*W(CO)4(SSCOCH2CH3)(1-)=((CH3CH2)4N)[W(CO)4(SSCOCH2CH3)]
922713-51-7

(CH3CH2)4N(1+)*W(CO)4(SSCOCH2CH3)(1-)=((CH3CH2)4N)[W(CO)4(SSCOCH2CH3)]

Conditions
ConditionsYield
In acetonitrile byproducts: NaCl, CO; under N2; Schlenk technique; mixt. of W compd. and Na salt in CH3CN refluxed for 2 h; evapn. under vac., residue dissolved in THF/acetone (10/1), filtration through silica/celite, filtrate evapd., residue washed with Et2O; elem. anal.;93%
3-(2-methylphenyl)prop-2-en-1-al
93614-78-9, 4549-82-0

3-(2-methylphenyl)prop-2-en-1-al

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

cyclohexylamine
108-91-8

cyclohexylamine

3-cyclohexyl-4-hydroxy-6-(2-methylphenyl)-1,3-thiazinane-2-thione

3-cyclohexyl-4-hydroxy-6-(2-methylphenyl)-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In chloroform at 61℃; for 1.83333h;92.7%
diisopropylammonium hydrogen sulphate
65087-26-5

diisopropylammonium hydrogen sulphate

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

diisopropyl-thiocarbamic acid S-ethyl ester
63644-60-0

diisopropyl-thiocarbamic acid S-ethyl ester

Conditions
ConditionsYield
Stage #1: diisopropylammonium hydrogen sulphate; sodium O-ethyl dithiocarbonate With dihydrogen peroxide In water at 45℃; for 1.5h; Green chemistry;
Stage #2: With sulfuric acid In water at 75℃; for 2.2h; pH=7; Green chemistry;
92%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

methylmercury(II) chloride
115-09-3

methylmercury(II) chloride

CH3Hg(S2COCH2CH3)
104855-65-4

CH3Hg(S2COCH2CH3)

Conditions
ConditionsYield
In dichloromethane MeHgCl dissolved in CH2Cl2 was treated with ligand, stirred at room temp. for 1 h; filtered, evapd. in open air, redissolved in CH2Cl2, filtered, covered with petroleum ether, crystd. in reflrigerator, filtered, dried in vacuo;elem. anal.;91.7%
hexan-1-amine
111-26-2

hexan-1-amine

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

3-(4-methylphenyl)acrylaldehyde
1504-75-2

3-(4-methylphenyl)acrylaldehyde

3-n-hexyl-4-hydroxy-6-(4-methylphenyl)-1,3-thiazinane-2-thione

3-n-hexyl-4-hydroxy-6-(4-methylphenyl)-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In methanol at 65℃; for 1.08333h;91.7%
sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

4-methoxy-aniline
104-94-9

4-methoxy-aniline

jasminaldehyde
122-40-7

jasminaldehyde

5-pentyl-3-(4-methoxyphenyl)-4-hydroxy-6-phenyl-1,3-thiazinane-2-thione

5-pentyl-3-(4-methoxyphenyl)-4-hydroxy-6-phenyl-1,3-thiazinane-2-thione

Conditions
ConditionsYield
In dichloromethane at 25℃; for 1.66667h;90.7%
((Pd(μ-I)((CH2)2S(O)Me))2)

((Pd(μ-I)((CH2)2S(O)Me))2)

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

Pd{(CH2)2(SO)(CH3)}(S2COC2H5)

Pd{(CH2)2(SO)(CH3)}(S2COC2H5)

Conditions
ConditionsYield
In dichloromethane Addn. of org. compd. to suspn. of Pd-complex (CH2Cl2) using n-Bu4NI as phase transfer catalyst and stirring. The yellow solid is dissolved within 6 min.; Washing of ppt. with H2O (3 times), removal of solvent, recrystn. of residue from n-hexane/CH2Cl2, elem. anal.;90%
In dichloromethane Addn. of org. compd. to suspn. of Pd-complex (CH2Cl2) and stirring. The yellow solid is dissolved within 15 min.;79%

140-90-9Relevant articles and documents

Supramolecular interactions in sodium N-(ethoxythioxomethyl)-β- alaninate-water (4/6) crystal and its application in synthesis of L-carnosine

Zhang, Shi-Jie,Xu, Feng,Yang, Wei-Ji,Hu, Wei-Xiao

, p. 1182 - 1189 (2012)

Compound sodium N-(ethoxythioxomethyl)-β-alaninate (sodium 3-(ethoxycarbonothioyl)propanoate) was synthesized and characterized by IR, 1HNMR, ESI-HRMS and single crystalX-ray diffraction. Single crystalX-ray diffraction analysis showed that the title compound crystallized in the triclinic space group P-1 with cell parameters a = 10.142 (2) A, b = 13.738 (3) A, c = 15.751 (3) A, α= 72.937 (2)°, β = 78.694 (2)°, γ = 89.999 (2)°, V = 2053.4 (7) A3, Dc = 1.464 g cm-3, Z = 2. In the extended structure of sodium N-(ethoxythioxomethyl)-β-alaninate-water (4/6), (NaL)4· 6H2O [L = CH3CH2OC(S)NHCH2CH 2COO], ligands (Ls) are stabilized by intermolecular O-H···O, N-H···O, C- H···O and weak O-H···S and C-H···S linkages, which further consolidate the crystal packing, making the ligand chains stacked along [0-1 1], and intramolecular O-H···S hydrogen bond is also observed. Each Na atom is surrounded with six O atoms, forming an octahedron and mutually bonded as tetramers. These tetramers are linked through O atom bridges from water molecules, extending as layers in the ab plane. In addition, synthesis of β-alanyl dipeptides was developed with particular focus on the preparation of L-carnosine. Springer Science+Business Media New York 2012.

The synthesis of iron sulfide nanocrystals from tris(O-alkylxanthato) iron(III) complexes

Akhtar, Masood,Malik, Mohammad Azad,Tuna, Floriana,O'Brien, Paul

, p. 8766 - 8774 (2013)

Tris(O-alkylxanthato)iron(iii) complexes (alkyl = Me (1), Et (2), and iBu (3)) were used as single source precursors for the synthesis of iron sulfide nanocrystals by thermolysis in oleylamine, hexadecylamine and octadecylamine at 170 to 300 °C. The morphology of the crystallites was strongly affected by the reaction conditions as well as the type of precursor used.

A thiadiazole compounds and its synthetic method

-

Paragraph 0032; 0039; 0040; 0041; 0059; 0066; 0067; 0068, (2019/02/02)

The invention relates to a thiadiazole compound and a synthesis method thereof. Alkoxy sodium xanthate is synthesized from an alcohol compound, sodium hydroxide and carbon disulfide, alkoxy thiocarbonyl hydrazine is synthesized from alkoxy sodium xanthate and hydrazine hydrate, and N'-alkoxyl thiocarbonyl-N-2-chloroacetylhydrazide is synthesized from alkoxy thiocarbonyl hydrazine and 2-chloroacetyl chloride; 2-alkoxyl-5-chloromethyl-1,3,4-thiadiazole is synthesized through cyclization of the generated hydrazide compound under an action of concentrated sulfuric acid and then undergoes a reaction with 4,5-dichloro-3(2H)pyridazinone, and the generated intermediate undergoes a substitution reaction with aliphatic amine or cyclic aliphatic amine or propyl sulfhydrate under catalysis of an alkaline reagent to synthesize a bishydrazide derivative. Compared with the prior art, the thiadiazole compound has the advantages of simple technological process and wide application range, is suitable for use in prevention and treatment of sanitary pests such as flies, mosquitoes, fleas and the like and prevention and treatment of other agricultural pests such as rice water weevils, beet armyworm, plutella xylostella, armyworm and the like, and is an insecticide having an application prospect.

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