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14593-46-5 Usage

Chemical Properties

Cream or light tan powder

Uses

Sodium tert-pentyloxide is a effective base for the alkylation of ketones.

Check Digit Verification of cas no

The CAS Registry Mumber 14593-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,9 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14593-46:
(7*1)+(6*4)+(5*5)+(4*9)+(3*3)+(2*4)+(1*6)=115
115 % 10 = 5
So 14593-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H11O.Na/c1-4-5(2,3)6;/h4H2,1-3H3;/q-1;+1

14593-46-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L15112)  Sodium tert-pentyloxide, 95%   

  • 14593-46-5

  • 25g

  • 284.0CNY

  • Detail
  • Alfa Aesar

  • (L15112)  Sodium tert-pentyloxide, 95%   

  • 14593-46-5

  • 100g

  • 586.0CNY

  • Detail
  • Aldrich

  • (752096)  Sodiumtert-pentoxidesolution  40% in toluene

  • 14593-46-5

  • 752096-100ML

  • 755.82CNY

  • Detail
  • Aldrich

  • (752096)  Sodiumtert-pentoxidesolution  40% in toluene

  • 14593-46-5

  • 752096-500ML

  • 2,811.51CNY

  • Detail
  • Aldrich

  • (280704)  Sodiumtert-pentoxide  95%

  • 14593-46-5

  • 280704-100G

  • 723.06CNY

  • Detail
  • Aldrich

  • (280704)  Sodiumtert-pentoxide  95%

  • 14593-46-5

  • 280704-500G

  • 3,005.73CNY

  • Detail
  • Aldrich

  • (702765)  Sodiumtert-pentoxidesolution  1.4 M in THF

  • 14593-46-5

  • 702765-100ML

  • 1,125.54CNY

  • Detail
  • Aldrich

  • (702765)  Sodiumtert-pentoxidesolution  1.4 M in THF

  • 14593-46-5

  • 702765-500ML

  • 3,594.24CNY

  • Detail

14593-46-5SDS

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 tert-pentoxide

1.2 Other means of identification

Product number -
Other names sodium tert-butylate

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:14593-46-5 SDS

14593-46-5Synthetic route

tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

Conditions
ConditionsYield
With sodium In n-heptane Inert atmosphere; Schlenk technique; Reflux;68.6%
With sodium In toluene for 24h; Heating;
With sodium In tetrahydrofuran; n-heptane
tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

FeCl3*6H2O

FeCl3*6H2O

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

Conditions
ConditionsYield
With sodium In tert-butyl alcohol
C36H49AgN2O3S

C36H49AgN2O3S

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

C34H53AgN2O

C34H53AgN2O

Conditions
ConditionsYield
In tetrahydrofuran; benzene for 1h; Inert atmosphere;96%
C35H47AgN2O3S

C35H47AgN2O3S

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

C33H51AgN2O

C33H51AgN2O

Conditions
ConditionsYield
In tetrahydrofuran; benzene for 1h; Inert atmosphere;96%
C21H26AuClN2

C21H26AuClN2

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

C26H37AuN2O

C26H37AuN2O

Conditions
ConditionsYield
In toluene for 4h; Schlenk technique; Inert atmosphere;90%
diiodomethane
75-11-6

diiodomethane

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

di-tert-pentyloxymethane
54699-28-4

di-tert-pentyloxymethane

Conditions
ConditionsYield
at 100 - 120℃;85%
4-acetylmorpholine
1696-20-4

4-acetylmorpholine

tert-Amyl alcohol
75-85-4

tert-Amyl alcohol

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

4-chloro-3',4'-dimethoxy benzophenone
116412-83-0

4-chloro-3',4'-dimethoxy benzophenone

dimethomorph

dimethomorph

Conditions
ConditionsYield
With carbon dioxide In 5,5-dimethyl-1,3-cyclohexadiene; di-isopropyl ether; paraffin oil82.2%
benzoic acid methyl ester
93-58-3

benzoic acid methyl ester

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

2-Benzoylcyclohexanone
3580-38-9

2-Benzoylcyclohexanone

Conditions
ConditionsYield
With Isopropylbenzene; sulfuric acid In water; cyclohexanone; sodium hydrogencarbonate76%
methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate

methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

cyanogen chloride
506-77-4

cyanogen chloride

methyl 4-(4-fluorophenyl)-6-isopropyl-2-(N-methanesulphonyl-N-methylamino)pyrimidine-5-carboxylate
289042-11-1

methyl 4-(4-fluorophenyl)-6-isopropyl-2-(N-methanesulphonyl-N-methylamino)pyrimidine-5-carboxylate

Conditions
ConditionsYield
In water74.1%
Methyl stearate
112-61-8

Methyl stearate

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

acetophenone
98-86-2

acetophenone

stearoylbenzoylmethane
58446-52-9

stearoylbenzoylmethane

Conditions
ConditionsYield
With sulfuric acid In water; sodium hydrogencarbonate74%
t-butyltris(N-methylacetamido)tin(IV)

t-butyltris(N-methylacetamido)tin(IV)

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

C19H42O3Sn

C19H42O3Sn

Conditions
ConditionsYield
In pentane for 16h; Inert atmosphere; Glovebox;66%
5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine
933784-97-5

5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine

[1,1'-bis(diphenylphosphino)ferrocene]-dichloropalladium

[1,1'-bis(diphenylphosphino)ferrocene]-dichloropalladium

1,1'-bis(diphenylphosphino)ferrocene)-dichloropalladium

1,1'-bis(diphenylphosphino)ferrocene)-dichloropalladium

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene
161265-03-8

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene

N-(2,5-difluoro-4-(morpholinomethyl)phenyl)-5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine
1252575-64-6

N-(2,5-difluoro-4-(morpholinomethyl)phenyl)-5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine

Conditions
ConditionsYield
In dichloromethane; water; toluene64%
sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

(S)-3-(1,3-benzodioxol-5-yl)-2,3-dihydro-6-propoxy-1H-indan-1-one
190969-66-5

(S)-3-(1,3-benzodioxol-5-yl)-2,3-dihydro-6-propoxy-1H-indan-1-one

(1S-trans)-methyl 1-(1,3-benzodioxol-5-yl)-2,3-dihydro-3-oxo-5-propoxy-1H-indene-2-carboxylate

(1S-trans)-methyl 1-(1,3-benzodioxol-5-yl)-2,3-dihydro-3-oxo-5-propoxy-1H-indene-2-carboxylate

Conditions
ConditionsYield
With sodium hydrogencarbonate; acetic acid In methanol; water; toluene62%
5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine
933784-97-5

5-fluoro-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine

4-(4-bromo-3-fluorobenzyl)morpholine
897016-96-5

4-(4-bromo-3-fluorobenzyl)morpholine

[1,1'-bis(diphenylphosphino)ferrocene]-dichloropalladium

[1,1'-bis(diphenylphosphino)ferrocene]-dichloropalladium

1,1'-bis(diphenylphosphino)ferrocene)-dichloropalladium

1,1'-bis(diphenylphosphino)ferrocene)-dichloropalladium

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene
161265-03-8

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene

5-fluoro-N-(2-fluoro-4-(morpholinomethyl)phenyl)-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine
1252575-59-9

5-fluoro-N-(2-fluoro-4-(morpholinomethyl)phenyl)-4-(2-methyl-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazol-5-yl)pyrimidin-2-amine

Conditions
ConditionsYield
In dichloromethane; water; toluene61%
carbon monoxide
201230-82-2

carbon monoxide

cyclooctyl chloride
1556-08-7

cyclooctyl chloride

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

A

cyclooctylcarboxaldehyde
6688-11-5

cyclooctylcarboxaldehyde

B

cyclooctanecarboxylic acid
4103-15-5

cyclooctanecarboxylic acid

C

Cyclooctanecarboxylic acid 1,1-dimethyl-propyl ester

Cyclooctanecarboxylic acid 1,1-dimethyl-propyl ester

Conditions
ConditionsYield
With iron(III) chloride; sodium hydride In 1,2-dimethoxyethane at 65℃; for 14h; Product distribution; C8H15Cl/FeCl3=10, C85H15Cl/NaH/Am-t-ONa/FeCl3=10/40/20/1 mmol;A 21%
B 48%
C 31%
4-bromo-2-chlorobenzoic acid methyl ester
185312-82-7

4-bromo-2-chlorobenzoic acid methyl ester

1-methyl-piperazine
109-01-3

1-methyl-piperazine

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

A

2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester
1059705-62-2

2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester

B

tert-pentyl 2-chloro-4-(4-methylpiperazin-1-yl)benzoate
1059705-74-6

tert-pentyl 2-chloro-4-(4-methylpiperazin-1-yl)benzoate

C

methyl 4-(4-methylpiperazin-1-yl)-2-(tert-pentyloxy)benzoate

methyl 4-(4-methylpiperazin-1-yl)-2-(tert-pentyloxy)benzoate

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride In tetrahydrofuran at 100℃; for 4h;A 38%
B n/a
C n/a
1-methyl-piperazine
109-01-3

1-methyl-piperazine

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

methyl 5-bromo-2-chloro-benzoate
251085-87-7

methyl 5-bromo-2-chloro-benzoate

A

C13H17ClN2O2
1059705-49-5

C13H17ClN2O2

B

C17H25ClN2O2

C17H25ClN2O2

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride In tetrahydrofuran at 100℃; for 4h;A 38%
B n/a
2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester
1059705-62-2

2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

benzylamine
100-46-9

benzylamine

A

2-Benzylamino-4-(4-methyl-piperazin-1-yl)-benzoic acid methyl ester

2-Benzylamino-4-(4-methyl-piperazin-1-yl)-benzoic acid methyl ester

B

tert-pentyl 2-(benzylamino)-4-(4-methylpiperazin-1-yl)benzoate
1059705-63-3

tert-pentyl 2-(benzylamino)-4-(4-methylpiperazin-1-yl)benzoate

Conditions
ConditionsYield
With 2-P(t-Bu)2-biphenyl; tris(dibenzylideneacetone)dipalladium (0) In toluene at 110℃; for 20h;A 38%
B 9%
1-methyl-piperazine
109-01-3

1-methyl-piperazine

4-bromo-2-chloro-1-nitrobenzene
89465-97-4

4-bromo-2-chloro-1-nitrobenzene

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

A

1-(3-chloro-4-nitrophenyl)-4-methylpiperazine
1059705-52-0

1-(3-chloro-4-nitrophenyl)-4-methylpiperazine

B

C11H14ClNO3

C11H14ClNO3

Conditions
ConditionsYield
With 1,1'-bis-(diphenylphosphino)ferrocene; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride In tetrahydrofuran at 100℃; for 4h;A 37%
B n/a
2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester
1059705-62-2

2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

phenethylamine
64-04-0

phenethylamine

A

4-(4-Methyl-piperazin-1-yl)-2-phenethylamino-benzoic acid methyl ester
897027-10-0

4-(4-Methyl-piperazin-1-yl)-2-phenethylamino-benzoic acid methyl ester

B

C25H35N3O2

C25H35N3O2

Conditions
ConditionsYield
With 2-P(t-Bu)2-biphenyl; tris(dibenzylideneacetone)dipalladium (0) In toluene at 110℃; for 20h;A 30%
B n/a
2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester
1059705-62-2

2-chloro-4-(4-methylpiperazin-1-yl)benzoic acid methyl ester

furan-2-ylmethanamine
617-89-0

furan-2-ylmethanamine

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

A

[1092]2-[(Furan-2-ylmethyl)-amino]-4-(4-methyl-piperazin-1-yl)-benzoic acid methyl ester
897027-11-1

[1092]2-[(Furan-2-ylmethyl)-amino]-4-(4-methyl-piperazin-1-yl)-benzoic acid methyl ester

B

tert-pentyl 2-((furan-2-ylmethyl)amino)-4-(4-methylpiperazin-1-yl)benzoate
1059705-64-4

tert-pentyl 2-((furan-2-ylmethyl)amino)-4-(4-methylpiperazin-1-yl)benzoate

Conditions
ConditionsYield
With 2-P(t-Bu)2-biphenyl; tris(dibenzylideneacetone)dipalladium (0) In toluene at 110℃; for 20h;A 21%
B 4%
C13H17ClN2O2
1059705-49-5

C13H17ClN2O2

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

benzylamine
100-46-9

benzylamine

A

C20H25N3O2

C20H25N3O2

B

C24H33N3O2

C24H33N3O2

Conditions
ConditionsYield
With 2-P(t-Bu)2-biphenyl; tris(dibenzylideneacetone)dipalladium (0) In toluene at 110℃; for 20h;A 16%
B n/a
{(C(OCH3)C(CH3)CH2)}pentacarbonyltungsten

{(C(OCH3)C(CH3)CH2)}pentacarbonyltungsten

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

A

{(tris(CH3CH2C(CH3)2OCH2C(CH3)CH2C(CH3)CH(OCH3))C(CH3O))}pentacarbonyltungsten

{(tris(CH3CH2C(CH3)2OCH2C(CH3)CH2C(CH3)CH(OCH3))C(CH3O))}pentacarbonyltungsten

B

{(μ-(CH3CH2C(CH3)2O(CH2C(CH3))4(CH(CH3O))(C(CH3O))3))}(pentacarbonyltungsten)3

{(μ-(CH3CH2C(CH3)2O(CH2C(CH3))4(CH(CH3O))(C(CH3O))3))}(pentacarbonyltungsten)3

C

{(μ-(CH3CH2C(CH3)2OCH2C(CH3)CH2CH(CH3))(C(CH3O))2)}(pentacarbonyl)2ditungsten

{(μ-(CH3CH2C(CH3)2OCH2C(CH3)CH2CH(CH3))(C(CH3O))2)}(pentacarbonyl)2ditungsten

D

{(tris(CH3CH2C(CH3)2OCH2CH(CH3))C(CH3O))}pentacarbonyltungsten

{(tris(CH3CH2C(CH3)2OCH2CH(CH3))C(CH3O))}pentacarbonyltungsten

Conditions
ConditionsYield
With hydrogenchloride In tetrahydrofuran; diethyl ether To a cooled (-78°C) suspension of C2H5(CH3)2CONa is added a precooled soln. (same temp.) of (CO)5W(C(OCH3)C(CH3)CH2) over 10 min, stirring (5 h, -78°C.), quencheing with precooled (same temp.) HCl/diethylether in THF, warming to room temp.; Solvent is removed under aspirator vac., residue is chromd. on silica gel, column is washed with hexane, CH2Cl2/hexane and ethyl acetate/hexane, evapn., distn. and recrystn. respectively, elem. anal.;A <1
B 15%
C <1
D 1%
thiophene
188290-36-0

thiophene

n-pentylsodium
1822-71-5

n-pentylsodium

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

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

methylammonium carbonate

Thiophene-2,5-dicarboxylic acid
4282-31-9

Thiophene-2,5-dicarboxylic acid

Conditions
ConditionsYield
aufeinanderfolgender Umsetzung;
sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

prenyl bromide
870-63-3

prenyl bromide

(3-methyl-but-2-enyl)-tert-pentyl ether
103754-95-6

(3-methyl-but-2-enyl)-tert-pentyl ether

chlorure d'acide ethyl-2 butyrique
2736-40-5

chlorure d'acide ethyl-2 butyrique

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

tert-pentyl-2-ethylbutanoate
100534-04-1

tert-pentyl-2-ethylbutanoate

Conditions
ConditionsYield
With diethyl ether
cyclohexa-1,4-diene
1165952-92-0

cyclohexa-1,4-diene

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

cyclohexa-1,3-diene
1165952-91-9

cyclohexa-1,3-diene

Conditions
ConditionsYield
at 150℃;
(R)-1-phenylethanol
1517-69-7

(R)-1-phenylethanol

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

(+)-(R)-methoxyphenylethane
52224-89-2

(+)-(R)-methoxyphenylethane

Conditions
ConditionsYield
With toluene; methyl iodide at 30 - 35℃;
5-chloro-5-phenyl-valeric acid ethyl ester
100607-73-6

5-chloro-5-phenyl-valeric acid ethyl ester

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

(E)-ethyl 5-phenylpent-4-enoate
22768-07-6, 121746-04-1, 93845-04-6

(E)-ethyl 5-phenylpent-4-enoate

Conditions
ConditionsYield
With benzene zuletzt unter Erwaermen;
7a,8,8a,9-tetrahydro-cyclopropa[b]phenanthren-7-one
109501-02-2

7a,8,8a,9-tetrahydro-cyclopropa[b]phenanthren-7-one

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

8,9-dihydro-cyclohepta[a]naphthalen-7-one
109500-98-3

8,9-dihydro-cyclohepta[a]naphthalen-7-one

Conditions
ConditionsYield
With benzene
benzyl bromide
100-39-0

benzyl bromide

sodium tert-pentoxide
14593-46-5

sodium tert-pentoxide

cyclopentanone
120-92-3

cyclopentanone

2,2-dibenzylcyclopentanone
57772-75-5

2,2-dibenzylcyclopentanone

Conditions
ConditionsYield
With diethyl ether; benzene anschliessendes Erhitzen auf Siedetemperatur;

14593-46-5Upstream product

14593-46-5Relevant articles and documents

N-Alkylation of 2-methoxy-10H-phenothiazine revisited. A facile entry to diversely N-substituted phenothiazine-coumarin hybrid dyes

Quesneau, Valentin,Renault, Kévin,Laly, Myriam,Jenni, Sébastien,Ponsot, Flavien,Romieu, Anthony

, (2020)

N-Alkylation of 2-methoxy-10H-phenothiazine, a valuable building block for the synthesis of bioactive compounds and reaction-based fluorescent probes, has been revisited aimed at introducing a substituent easily convertible into cationic or zwitterionic side chains. We focused our attention on the 3-dimethylaminopropyl group since its derivatization through reactions with various alkyl halides or sultones is a well-established and effective way to enhance polarity of diverse hydrophobic molecular scaffolds. This two-step functionalization approach was applied to the synthesis of novel phenothiazine-coumarin hybrid dyes whose spectral features, especially their NIR-I emission, have been determined in aqueous media with the ultimate goal of identifying novel fluorescent markers for bioanalytical applications, including fluorogenic detection of reactive oxygen species (ROS) through selective S-oxidation reaction of phenothiazine scaffold.

Preparation method for low residual granular sodium alkoxide or potassium alcoholate

-

Paragraph 0043-0044, (2017/01/17)

The invention provides a preparation method for low residual granular sodium alkoxide or potassium alcoholate. The method includes using sodium or potassium and alcohol as raw materials, mixing the mixture with a solvent, reacting in inert gas atmosphere by using a microwave heating method, and removing the residual alcohol and solvent in the presence of microwave after the reaction to get the granular sodium alkoxide or potassium alcoholate. The microwave frequency is 2450 +/- 50 MHz. The method can prepare sodium alkoxide or potassium alcoholate with low residual solvent, and the prepared sodium alkoxide or potassium alcoholate is large granular solid, so that the development from powdered product to granular product can be realized, and the problems of residual solvent and potential risk troubled human for a long time can be overcome.

Fluorescent diketopyrrolopyrroles

-

, (2008/06/13)

The present invention relates to fluorescent diketopyrrolopyrroles of formula I and processes for its preparation, its uses and compositions comprising the compounds of formula I.

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