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623-79-0

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623-79-0 Usage

General Description

O,S-Diethyl dithiocarbonate is a chemical compound used mainly as a reagent in organic synthesis and medicine production. This organosulfur compound is usually hydrolyzed with water, producing ethanol and carbon disulfide. It has a molecular formula of (C2H5O)2CS2 and usually comes as a yellow liquid with a characteristic odor. O,S-Diethyl dithiocarbonate is incompatible with strong oxidizing agents, and it must be handled with care due to its high flammability risk. Despite its wide usage in industry, there are health risks associated with this chemical, such as skin irritations, eye damage, respiratory irritation, and potential adverse environmental effects. Therefore, proper safety measures should be taken during handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 623-79-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 623-79:
(5*6)+(4*2)+(3*3)+(2*7)+(1*9)=70
70 % 10 = 0
So 623-79-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H10OS2/c1-3-6-5(7)8-4-2/h3-4H2,1-2H3

623-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name O,S-Diethyl dithiocarbonate

1.2 Other means of identification

Product number -
Other names ethyl-xanthogenic acid ethylester

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:623-79-0 SDS

623-79-0Synthetic route

diethyl sulfate
64-67-5

diethyl sulfate

potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With sodium hydrogencarbonate In water for 1.5h; Ambient temperature;93%
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

ethyl iodide
75-03-6

ethyl iodide

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
18-crown-6 ether In dichloromethane for 1h; Ambient temperature;82%
In ethanol for 2h; Heating;55%
With ethanol
bis(ethoxythiocarbonyl) sulfide
2905-52-4

bis(ethoxythiocarbonyl) sulfide

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
In toluene Heating; Irradiation;69%
Zersetzen;
In toluene for 0.0833333h; Heating; Irradiation; Yield given;
S-(ethoxycarbonyl) O-ethyl dithiocarbonate
3278-35-1

S-(ethoxycarbonyl) O-ethyl dithiocarbonate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
In n-heptane for 2.5h; Heating; Irradiation;59%
Heating; Irradiation;59%
In toluene Heating; Irradiation;
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

cyclooctatetraene dibromide

cyclooctatetraene dibromide

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

(4Z,6Z,8Z)-(3aS,9aR)-3a,9a-Dihydro-cycloocta[1,3]dithiol-2-one

(4Z,6Z,8Z)-(3aS,9aR)-3a,9a-Dihydro-cycloocta[1,3]dithiol-2-one

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Conditions
ConditionsYield
In acetone for 22h; Ambient temperature; Yield given. Further byproducts given;A 11%
B n/a
C 30%
D 12%
In acetone for 22h; Ambient temperature; Further byproducts given;A 11%
B n/a
C 30%
D 12%
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

cyclooctatetraene dibromide

cyclooctatetraene dibromide

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Dithiocarbonic acid S-((1R,2R,7R,8S)-8-bromo-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1R,2R,7R,8S)-8-bromo-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Conditions
ConditionsYield
In acetone for 22h; Ambient temperature; Further byproducts given;A 11%
B 1.6%
C 30%
D 12%
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Dithiocarbonic acid S-((1R,2R,7R,8S)-8-bromo-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1R,2R,7R,8S)-8-bromo-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((7R,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[4.2.0]octa-2,4-dien-7-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Dithiocarbonic acid S-((1S,2S,7S,8R)-8-ethoxythiocarbonylsulfanyl-bicyclo[5.1.0]octa-3,5-dien-2-yl) ester O-ethyl ester

Conditions
ConditionsYield
With 7,8-Dibromobicyclo<4.2.0>octa-2,4-diene In N,N-dimethyl-formamide for 18h; Ambient temperature; Further byproducts given;A 29%
B n/a
C 25%
D 10%
ethyl bromide
74-96-4

ethyl bromide

potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With ethanol
In ethanol
In acetone Heating;
With ethanol for 4h; Esterification; Heating;
In ethanol for 4h; Heating;
chloroethane
75-00-3

chloroethane

potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With ethanol
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

A

carbon disulfide
75-15-0

carbon disulfide

B

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

C

thiocarbonic acid O,O'-diethyl ester
762-03-8

thiocarbonic acid O,O'-diethyl ester

D

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

Conditions
ConditionsYield
bei der Destillation; Produkt 5:Schwefel;
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 200 - 210℃;
Zersetzen;
bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

thiocarbonic acid O,O'-diethyl ester
762-03-8

thiocarbonic acid O,O'-diethyl ester

Conditions
ConditionsYield
bei der Destillation;
bis-ethoxythiocarbonyl-trisulfane
1851-77-0

bis-ethoxythiocarbonyl-trisulfane

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 135℃; Zersetzen;
bis(ethoxythiocarbonyl) tetrasulfide
1851-71-4

bis(ethoxythiocarbonyl) tetrasulfide

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 135℃; Zersetzen;
2-methyl-5-nitrobenzene-1-sulfonyl chloride
121-02-8

2-methyl-5-nitrobenzene-1-sulfonyl chloride

potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

bis-ethoxythiocarbonyldisulfane
502-55-6

bis-ethoxythiocarbonyldisulfane

Conditions
ConditionsYield
Erhitzen unter vermindertem Druck;
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With benzenesulfonyl chloride
With p-toluenesulfonyl chloride
With 2-Naphthalenesulfonyl chloride
With 2-Naphthalenesulfonyl chloride at 100℃;
With 5-diazonio-6-nitroindan chloride
potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

benzenesulfonyl chloride
98-09-9

benzenesulfonyl chloride

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

diphenyl disulfone
10409-06-0

diphenyl disulfone

C

potassium benzenesulfonate
934-55-4

potassium benzenesulfonate

Conditions
ConditionsYield
at 0℃; analoge Reaktion mit anderen Sulfonsaeurechloriden;
diethyl dibromomalonate
631-22-1

diethyl dibromomalonate

potassium ethyl xanthogenate
140-89-6

potassium ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With 2,3-dimethyl-buta-1,3-diene
bis(ethoxythiocarbonyl) sulfide
2905-52-4

bis(ethoxythiocarbonyl) sulfide

bis-(2,2,2-trimethylethyl) xanthic anhydride
126078-75-9

bis-(2,2,2-trimethylethyl) xanthic anhydride

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

Dithiocarbonic acid O-(2,2-dimethyl-propyl) ester S-ethyl ester

Dithiocarbonic acid O-(2,2-dimethyl-propyl) ester S-ethyl ester

C

Dithiocarbonic acid S-(2,2-dimethyl-propyl) ester O-ethyl ester

Dithiocarbonic acid S-(2,2-dimethyl-propyl) ester O-ethyl ester

D

O,S-di-(2,2,2-trimethylethyl) dithiocarbonate
126078-76-0

O,S-di-(2,2,2-trimethylethyl) dithiocarbonate

Conditions
ConditionsYield
In toluene Irradiation; Title compound not separated from byproducts;
bis-ethyl xanthogen

bis-ethyl xanthogen

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
under 15 Torr; bei der Destillation;
copper xanthogenate

copper xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 350℃;
dinitroso-iron(II)-ethyl xanthogenate

dinitroso-iron(II)-ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 50 - 60℃; im Hochvakuum;
mercury xanthogenate

mercury xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 350℃;
nickel ethyl xanthogenate

nickel ethyl xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 350℃;
silver xanthogenate

silver xanthogenate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
at 350℃;
ethyl isothiocyanate
542-90-5

ethyl isothiocyanate

sulfuric acid
7664-93-9

sulfuric acid

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

carbon dioxide
124-38-9

carbon dioxide

C

ammonia
7664-41-7

ammonia

ethyl isothiocyanate
542-90-5

ethyl isothiocyanate

sulfuric acid
7664-93-9

sulfuric acid

A

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

B

carbon dioxide
124-38-9

carbon dioxide

C

ammonia
7664-41-7

ammonia

D

sulfur dioxide

sulfur dioxide

Conditions
ConditionsYield
beim Erhitzen;
cuprous ethyl xanthate

cuprous ethyl xanthate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
In neat (no solvent) decompn. at 350°C;;
ethyl bromide
74-96-4

ethyl bromide

sodium O-ethyl dithiocarbonate
140-90-9

sodium O-ethyl dithiocarbonate

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Conditions
ConditionsYield
With N-benzyl-N,N,N-triethylammonium chloride In methanol; water at 20 - 25℃;
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

S,S-diethyl dithiocarbonate
623-80-3

S,S-diethyl dithiocarbonate

Conditions
ConditionsYield
Aliquat 336 at 100℃; for 1h;85%
With boron trifluoride diethyl etherate In diethyl ether for 1.5h; Heating;65%
With aluminium trichloride In carbon disulfide Heating;
With boron trifluoride diethyl etherate
With 4-(dimethylamino)pyridine N-oxide In dimethylsulfoxide-d6 at 80℃; for 3h;88 % Spectr.
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

rac-Ala-OH
302-72-7

rac-Ala-OH

N-ethoxythioxomethyl-D,L-alanine
90010-88-1

N-ethoxythioxomethyl-D,L-alanine

Conditions
ConditionsYield
With sodium hydroxide In ethanol for 72h; Heating;82%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

benzylamine
100-46-9

benzylamine

benzylthiocarbamic acid O-ethyl ester
55365-86-1

benzylthiocarbamic acid O-ethyl ester

Conditions
ConditionsYield
for 8h; Heating;81%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

acetone
67-64-1

acetone

Acetothioacetic Acid O-Ethyl Ester
41500-02-1

Acetothioacetic Acid O-Ethyl Ester

Conditions
ConditionsYield
With sodium hydride In 1,2-dimethoxyethane 1) room temp., 1 h, 2) reflux, 4 h.;80%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

N-butylamine
109-73-9

N-butylamine

O-Ethyl N-Butylthiocarbamate
55365-85-0

O-Ethyl N-Butylthiocarbamate

Conditions
ConditionsYield
for 8h; Heating;75%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

C9H8BrN3O2

C9H8BrN3O2

ethyl 6-bromo-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

ethyl 6-bromo-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;58%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

C9H8ClN3O2

C9H8ClN3O2

ethyl 6-chloro-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

ethyl 6-chloro-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;54%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

methyl [1,2,3]triazolo[1,5-a]pyrazine-3-carboxylate

methyl [1,2,3]triazolo[1,5-a]pyrazine-3-carboxylate

methyl 3-oxo-3H-thiazolo[3,4-a]pyrazine-1-carboxylate

methyl 3-oxo-3H-thiazolo[3,4-a]pyrazine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;47%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

chloro(chlorosulfanyl)methanone
2757-23-5

chloro(chlorosulfanyl)methanone

A

(Ethyldithio)carbonyl Chloride
13221-50-6

(Ethyldithio)carbonyl Chloride

B

(((Ethylthio)carbonyl)dithio)carbonyl Chloride
87462-98-4

(((Ethylthio)carbonyl)dithio)carbonyl Chloride

Conditions
ConditionsYield
at 0℃; for 10h; Title compound not separated from byproducts;A 2%
B 46%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

ethyl 5-bromo-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate

ethyl 5-bromo-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate

ethyl 7-bromo-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

ethyl 7-bromo-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;46%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

methyl 5-methyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate

methyl 5-methyl-[1,2,3]triazolo[1,5-a]pyridine-3-carboxylate

methyl 7-methyl-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

methyl 7-methyl-3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;43%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

3-ethoxycarbonyltriazolo<1,5-a>pyridine
87838-54-8

3-ethoxycarbonyltriazolo<1,5-a>pyridine

ethyl 3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate
74376-31-1

ethyl 3-oxo-3H-thiazolo[3,4-a]pyridine-1-carboxylate

Conditions
ConditionsYield
With cobalt(II) 5,10,15,20-tetraphenylporphyrin In toluene at 120℃; Schlenk technique; Inert atmosphere;36%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

1-methoxy-4-dimethylaminopyridinium iodide

1-methoxy-4-dimethylaminopyridinium iodide

A

S,S-diethyl dithiocarbonate
623-80-3

S,S-diethyl dithiocarbonate

B

S-Ethyl S'-methyl dithiocarbonate
10596-55-1

S-Ethyl S'-methyl dithiocarbonate

Conditions
ConditionsYield
In dimethylsulfoxide-d6 at 80℃; for 30h; Mechanism; Product distribution;A 31.75%
B 4.7%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

A

S,S-diethyl dithiocarbonate
623-80-3

S,S-diethyl dithiocarbonate

B

S-Ethyl S'-methyl dithiocarbonate
10596-55-1

S-Ethyl S'-methyl dithiocarbonate

Conditions
ConditionsYield
1-methoxy-4-dimethylaminopyridinium iodide In dimethylsulfoxide-d6 at 80℃; for 30h; Title compound not separated from byproducts;A 31.75%
B 4.7%
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

ethylenediamine
107-15-3

ethylenediamine

N-butylamine
109-73-9

N-butylamine

A

N,N'-ethylenethiourea
96-45-7

N,N'-ethylenethiourea

B

2-(2'-Aminoethylamino)-Δ2-imidazoline
77988-96-6

2-(2'-Aminoethylamino)-Δ2-imidazoline

Conditions
ConditionsYield
for 6h; Mechanism; Heating;A 17.5%
B 18%
sarcosine
107-97-1

sarcosine

O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

N-(ethoxycarbonothioyl)-N-methylglycine
59857-32-8

N-(ethoxycarbonothioyl)-N-methylglycine

Conditions
ConditionsYield
With potassium hydroxide; ethanol
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

chloroamine-T
127-65-1

chloroamine-T

N,N'-bis-(toluene-4-sulfonyl)-ethanesulfinamidyne
81221-65-0

N,N'-bis-(toluene-4-sulfonyl)-ethanesulfinamidyne

Conditions
ConditionsYield
With water
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

5-aminomethyl-2-methyl-3H-pyrimidin-4-one; hydrochloride
934-25-8

5-aminomethyl-2-methyl-3H-pyrimidin-4-one; hydrochloride

(2-methyl-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-carbothioamidoic acid O-ethyl ester

(2-methyl-6-oxo-1,6-dihydro-pyrimidin-5-ylmethyl)-carbothioamidoic acid O-ethyl ester

Conditions
ConditionsYield
With sodium ethanolate
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

4-amino-5-thioxo-[1,2,4]triazolidin-3-one hydrazone
1750-12-5

4-amino-5-thioxo-[1,2,4]triazolidin-3-one hydrazone

Conditions
ConditionsYield
With water; hydrazine und anschliessenden Erhitzen mit wss.HCl;
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

O-ethyl thiocarbamate
625-57-0

O-ethyl thiocarbamate

Conditions
ConditionsYield
With ammonia
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

ethoxy(potassiosulfanyl)methanethione
35832-93-0

ethoxy(potassiosulfanyl)methanethione

Conditions
ConditionsYield
With potassium hydroxide; ethanol
O,S-Diethyl dithiocarbonate
623-79-0

O,S-Diethyl dithiocarbonate

Thiocarbohydrazide
2231-57-4

Thiocarbohydrazide

Conditions
ConditionsYield
With ethanol; hydrazine hydrate

623-79-0Relevant articles and documents

Dithiocarbonato nickel, palladium and platinum complexes bearing bis(diphenylphosphino)ferrocene: synthesis and X-ray structure determination

El-Khateeb, Mohammad,Tanash, Qusay,Abul-Futouh, Hassan,G?rls, Helmar,Weigand, Wolfgang

, (2019)

Abstract: The dithiocarbonato metal complexes M(κ2S,S-S2CO)(κ2P,P-dppf) {M= Ni, Pd, Pt; dppf= bis(diphenylphosphino)ferrocene} are obtained from the reaction of the metal(II) complexes [M(κ2S,S-S2COEt)2] with the dppf ligand or from the chloride substitution of M(κ2P,P-dppf)Cl2 by the O-ethyldithiocabonato anion. These complexes are produced by C-O bond cleavage by the O-ethyldithiocarbonato anion present in solution. These new complexes have been characterized by UV-Vis, NMR, IR spectroscopy and elemental analysis. The structures of the three complexes were further confirmed by single-crystal X-ray diffraction analysis. Graphical Abstract: The dithiocarbonato metal complexes M(κ2S,S-S2CO)(κ2P,P-dppf) {M= Ni, Pd, Pt, dppf= bis(diphenylphosphino)ferrocene} are obtained from the reaction of the metal(II) complexes [M(κ2S,S-S2COEt)2] with the dppf ligand or from the chloride substitution of M(κ2P,P-dppf)Cl2 by the O-ethyldithiocabonato anion. These new complexes have been characterized by UV-Vis, NMR, IR spectroscopy and elemental analysis. The structures of complexes 1–3 were further confirmed by single-crystal X-ray diffraction analysis.[Figure not available: see fulltext.].

Reihlen,Elben,Everet

, p. 45,50 (1931)

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 (2013/02/22)

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.

New radical reactions of S-alkoxycarbonyl xanthates. Total synthesis of (±)-cinnamolide and (±)-methylenolactocin

Forbes, Judith E.,Saicic, Radomir N.,Zard, Samir Z.

, p. 3791 - 3802 (2007/10/03)

Irradiation with visible light of S-alkoxycarbonyl xanthates derived from various alcohols gives rise to alkoxycarbonyl radicals with bifurcate reactivity: loss of carbon dioxide leads to deoxygenated derivatives (i.e. alkyl xanthates) whereas intramolecular addition to a suitably located double bond produces lactones; these new reactions were applied to the total synthesis of (±)-cinnamolide and (±)-methylenolactocin.

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