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5332-06-9 Usage

Chemical Properties

Colorless to yellow liquid

Uses

4-bromobutyronitrile is used as a precursor for the preparation of cylopropyl cyanide. Its derivative, 4-Bromo-2,2-Diphenyl Butyronitrile is used as an intermediate for loperamide.

Check Digit Verification of cas no

The CAS Registry Mumber 5332-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5332-06:
(6*5)+(5*3)+(4*3)+(3*2)+(2*0)+(1*6)=69
69 % 10 = 9
So 5332-06-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6BrN/c5-3-1-2-4-6/h1-3H2

5332-06-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A10674)  4-Bromobutyronitrile, 97%   

  • 5332-06-9

  • 10g

  • 529.0CNY

  • Detail
  • Alfa Aesar

  • (A10674)  4-Bromobutyronitrile, 97%   

  • 5332-06-9

  • 50g

  • 1761.0CNY

  • Detail
  • Alfa Aesar

  • (A10674)  4-Bromobutyronitrile, 97%   

  • 5332-06-9

  • 250g

  • 3842.0CNY

  • Detail

5332-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-BROMOBUTYRONITRILE

1.2 Other means of identification

Product number -
Other names 4-Bromobutanenitrile

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:5332-06-9 SDS

5332-06-9Synthetic route

4-bromobutyraldehyde
38694-47-2

4-bromobutyraldehyde

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With HCl·DMPU; hydroxylamine hydrochloride In acetonitrile at 60℃;76%
4-bromobut-2-enenitrile
42879-03-8

4-bromobut-2-enenitrile

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
Hydrogenation; 4-bromo-buten-(2)-oic acid (1)-nitrile, higher-melting form;
ethanol
64-17-5

ethanol

sodium cyanide
143-33-9

sodium cyanide

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

A

4-Chlorobutyronitrile
628-20-6

4-Chlorobutyronitrile

B

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

sodium cyanide
143-33-9

sodium cyanide

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With ethanol
potassium cyanide
151-50-8

potassium cyanide

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With ethanol
sodium cyanide
143-33-9

sodium cyanide

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With ethanol
potassium cyanide
151-50-8

potassium cyanide

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With ethanol
With methanol
1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-Chlorobutyronitrile
628-20-6

4-Chlorobutyronitrile

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With lithium bromide In various solvent(s) at 120℃; for 2h; Yield given;
higher-melting 4-bromo-crotononitrile

higher-melting 4-bromo-crotononitrile

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With acetic acid ester; palladium Hydrogenation;
lower-melting 4-bromo-crotononitrile

lower-melting 4-bromo-crotononitrile

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With acetic acid ester; palladium Hydrogenation;
potassium cyanide
151-50-8

potassium cyanide

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

A

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

B

trimethylene dicyanide

trimethylene dicyanide

Conditions
ConditionsYield
With ethanol; water Alkohol abdestillieren,Rueckstand mit Wasser versetzen und abgeschiedenes Oel fraktionieren;
4-bromobut-2-enenitrile
42879-03-8

4-bromobut-2-enenitrile

ethyl acetate
141-78-6

ethyl acetate

palladium

palladium

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
Hydrogenation; 4-bromo-buten-(2)-oic acid (1)-nitrile, lower-melting form;
2,5-diiodo-1,4-hydroquinone
13064-64-7

2,5-diiodo-1,4-hydroquinone

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
With hydrogenchloride; sodium hydroxide In N,N-dimethyl-formamide
potassium cyanide

potassium cyanide

1,3-chlorobromopropane
109-70-6

1,3-chlorobromopropane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
In ethanol; water for 2h; Reflux;16.9 g
sodium cyanide
773837-37-9

sodium cyanide

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

Conditions
ConditionsYield
In methanol; water at 55℃; for 8h; Large scale;
propan-1-ol-3-amine
156-87-6

propan-1-ol-3-amine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(3-Hydroxy-propylamino)-butyronitrile
159791-11-4

4-(3-Hydroxy-propylamino)-butyronitrile

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 20h; Heating;100%
With potassium carbonate; sodium iodide In acetonitrile for 20h; Alkylation; Heating;6.70 g
1-(2-Methoxyphenyl)piperazine
35386-24-4

1-(2-Methoxyphenyl)piperazine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4‐[4‐(2‐methoxyphenyl)piperazin‐1‐yl]butannitrile
25024-99-1

4‐[4‐(2‐methoxyphenyl)piperazin‐1‐yl]butannitrile

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone for 8h; Reflux;100%
With potassium carbonate; potassium iodide In acetone at 20℃; Reflux;100%
With sodium hydrogencarbonate In acetonitrile for 16h; Reflux;99%
4-(4-fluorophenyl)piperidine hydrochloride

4-(4-fluorophenyl)piperidine hydrochloride

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-[4-(4-fluorophenyl)-1-piperidinyl]butanenitrile
721958-42-5

4-[4-(4-fluorophenyl)-1-piperidinyl]butanenitrile

Conditions
ConditionsYield
With caesium carbonate; sodium iodide In acetonitrile at 60℃; for 24h;100%
sodium benzoate
532-32-1

sodium benzoate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-benzoyloxybutyronitrile
75272-93-4

4-benzoyloxybutyronitrile

Conditions
ConditionsYield
With tetra(n-butyl)ammonium hydrogensulfate In acetone for 4h; Molecular sieve; ethanol;100%
methyl 5-chloro-2-hydroxybenzoate
4068-78-4

methyl 5-chloro-2-hydroxybenzoate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

methyl 5-chloro-2-(3-cyanopropoxy)benzoate
1251927-29-3

methyl 5-chloro-2-(3-cyanopropoxy)benzoate

Conditions
ConditionsYield
With potassium carbonate In acetone for 48h; Reflux;100%
1-(tert-butoxycarbonyl)-4-aminopiperidine
87120-72-7

1-(tert-butoxycarbonyl)-4-aminopiperidine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(3-cyano-propylamino)-piperidine-1-carboxylic acid tert-butyl ester

4-(3-cyano-propylamino)-piperidine-1-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 48h; Reflux;100%
tert-butyl 4-(aminomethyl)piperidine-1-carboxylate
144222-22-0

tert-butyl 4-(aminomethyl)piperidine-1-carboxylate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

C15H27N3O2
1448687-26-0

C15H27N3O2

Conditions
ConditionsYield
With potassium carbonate In acetonitrile for 48h; Reflux;100%
4-[(5-methyl-3-phenylisoxazol-4-yl)methoxy]benzoic acid

4-[(5-methyl-3-phenylisoxazol-4-yl)methoxy]benzoic acid

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

3-cyanopropyl 4-[(5-methyl-3-phenylisoxazol-4-yl)methoxy]benzoate

3-cyanopropyl 4-[(5-methyl-3-phenylisoxazol-4-yl)methoxy]benzoate

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 96h; Inert atmosphere; Sealed tube;100%
2-Phenylimidazole
670-96-2

2-Phenylimidazole

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(2-phenyl-1H-imidazol-1-yl)butanenitrile
198549-12-1

4-(2-phenyl-1H-imidazol-1-yl)butanenitrile

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide99%
Stage #1: 2-Phenylimidazole With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.25h;
Stage #2: 4-bromobutanenitrile In N,N-dimethyl-formamide at 20℃;
99%
Stage #1: 2-Phenylimidazole With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere;
Stage #2: 4-bromobutanenitrile In N,N-dimethyl-formamide at 0 - 20℃; Inert atmosphere;
methyl 4-hydroxy-3-chlorobenzoate
3964-57-6

methyl 4-hydroxy-3-chlorobenzoate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

3-chloro-4-(4-nitrilobutoxy)-benzoic acid methyl ester

3-chloro-4-(4-nitrilobutoxy)-benzoic acid methyl ester

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide; butanone for 24h; Heating / reflux;99%
1-(3-Trifluoromethylphenyl)piperazine
15532-75-9

1-(3-Trifluoromethylphenyl)piperazine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(4-(3-(trifluoromethyl)phenyl)piperazin-1-yl)butanenitrile

4-(4-(3-(trifluoromethyl)phenyl)piperazin-1-yl)butanenitrile

Conditions
ConditionsYield
Stage #1: 1-(3-Trifluoromethylphenyl)piperazine With potassium carbonate; potassium iodide In acetonitrile at 20℃; for 0.0833333h; Inert atmosphere;
Stage #2: 4-bromobutanenitrile In acetonitrile for 14h; Sealed tube; Reflux; Inert atmosphere;
99%
With potassium carbonate In acetonitrile Heating / reflux;97%
With potassium carbonate In acetonitrile Reflux;97%
4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

sodium thiomethoxide
5188-07-8

sodium thiomethoxide

4-(methylthio)butyronitrile
59121-24-3

4-(methylthio)butyronitrile

Conditions
ConditionsYield
In methanol99%
In methanol at 20℃;93%
In methanol for 7h; Reflux;89%
1-(2,5-dimethylphenyl)piperazine
1013-25-8

1-(2,5-dimethylphenyl)piperazine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-[4-(2,5-dimethylphenyl)piperazin-1-yl]butanenitrile
1181802-58-3

4-[4-(2,5-dimethylphenyl)piperazin-1-yl]butanenitrile

Conditions
ConditionsYield
With sodium hydrogencarbonate In acetonitrile for 16h; Reflux;99%
2-(3-bromophenylthio)pyridine-3-ol
263390-44-9

2-(3-bromophenylthio)pyridine-3-ol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(2-(3-bromophenylthio)pyridin-3-yloxy)butanenitrile
1452773-17-9

4-(2-(3-bromophenylthio)pyridin-3-yloxy)butanenitrile

Conditions
ConditionsYield
With potassium carbonate In N,N-dimethyl-formamide at 80℃; for 5h; Mitsunobu Displacement;99%
ethyl 5-bromoindolecarboxylate
16732-70-0

ethyl 5-bromoindolecarboxylate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

ethyl 5-chloro-1-(3-cyanopropyl)-1H-indole-2-carboxylate
1513681-57-6

ethyl 5-chloro-1-(3-cyanopropyl)-1H-indole-2-carboxylate

Conditions
ConditionsYield
Stage #1: ethyl 5-bromoindolecarboxylate With caesium carbonate In acetonitrile at 20℃; for 0.5h;
Stage #2: 4-bromobutanenitrile In acetonitrile at 20℃;
99%
Ethyl 4-nitropyrrole-2-carboxylate
5930-92-7

Ethyl 4-nitropyrrole-2-carboxylate

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

ethyl 4-nitro-1-(3-cyanopropyl)pyrrole-2-carboxylate
1575816-22-6

ethyl 4-nitro-1-(3-cyanopropyl)pyrrole-2-carboxylate

Conditions
ConditionsYield
With potassium carbonate; potassium iodide In acetone for 0.5h; Reflux;99%
5-chloro-indole-2-carboxylic acid ethyl ester
4792-67-0

5-chloro-indole-2-carboxylic acid ethyl ester

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

ethyl 5-chloro-1-(3-cyanopropyl)-1H-indole-2-carboxylate
1513681-57-6

ethyl 5-chloro-1-(3-cyanopropyl)-1H-indole-2-carboxylate

Conditions
ConditionsYield
Stage #1: 5-chloro-indole-2-carboxylic acid ethyl ester With caesium carbonate In acetonitrile at 25℃; for 0.5h;
Stage #2: 4-bromobutanenitrile In acetonitrile at 25℃;
99%
With caesium carbonate In acetonitrile at 20℃;99%
Stage #1: 5-chloro-indole-2-carboxylic acid ethyl ester With caesium carbonate In acetonitrile for 0.5h;
Stage #2: 4-bromobutanenitrile In acetonitrile at 20℃;
99%
4-nitro-phenol
100-02-7

4-nitro-phenol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(4-nitrophenoxy)butanenitrile
99072-20-5

4-(4-nitrophenoxy)butanenitrile

Conditions
ConditionsYield
With potassium carbonate In acetone for 20h; Reflux;99%
2,4-dichlorophenol
120-83-2

2,4-dichlorophenol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(2,4-dichlorophenoxy)butanenitrile
63867-25-4

4-(2,4-dichlorophenoxy)butanenitrile

Conditions
ConditionsYield
With potassium carbonate In acetone for 20h; Reflux;99%
4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

cyclopropropanecarbonitrile
5500-21-0

cyclopropropanecarbonitrile

Conditions
ConditionsYield
With sodium In ethylene glycol at 20 - 50℃; for 0.25h; Temperature; Solvent; Reagent/catalyst;98%
With ammonia; sodium amide; ferric nitrate
With tetra(n-butyl)ammonium hydroxide In xylene at 40℃;
1H-imidazole
288-32-4

1H-imidazole

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-imidazol-1-ylbutyronitrile
72338-63-7

4-imidazol-1-ylbutyronitrile

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide98%
Stage #1: 1H-imidazole With sodium hydride In N,N-dimethyl-formamide at 0℃; for 0.25h;
Stage #2: 4-bromobutanenitrile In N,N-dimethyl-formamide at 20℃;
98%
With sodium methylate 1.) DMF, RT, 30 min, 2.) DMF, a) RT, 30 min, b) reflux, 1 h; Yield given. Multistep reaction;
3-((naphthalen-2-ylmethyl)amino)propan-1-ol
163083-82-7

3-((naphthalen-2-ylmethyl)amino)propan-1-ol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

N-(3-cyanopropyl)-N-(2-naphthylmethyl)-3-amino-1-propanol
163083-83-8

N-(3-cyanopropyl)-N-(2-naphthylmethyl)-3-amino-1-propanol

Conditions
ConditionsYield
With triethylamine In toluene for 3.5h; Alkylation; Heating;98%
5'-acetylthio-5'-deoxy-2',3'-O-isopropylidene adenosine
84365-04-8

5'-acetylthio-5'-deoxy-2',3'-O-isopropylidene adenosine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

5'-[3-(cyano)propylthio]-5'-deoxy-2',3'-O-isopropylideneadenosine
263715-53-3

5'-[3-(cyano)propylthio]-5'-deoxy-2',3'-O-isopropylideneadenosine

Conditions
ConditionsYield
With sodium methylate In water at 20℃; for 3.5h; Alkylation;98%
4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine
304863-12-5

1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine

3,8,13,18-tetrakis(mesitylenesulfonyl)-3,8,13,18-tetraazaheneicosanecyanide
304863-14-7

3,8,13,18-tetrakis(mesitylenesulfonyl)-3,8,13,18-tetraazaheneicosanecyanide

Conditions
ConditionsYield
Stage #1: 1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine With sodium hydride In N,N-dimethyl-formamide for 0.5h;
Stage #2: 4-bromobutanenitrile In N,N-dimethyl-formamide at 22℃; for 18h;
98%
piperidine
110-89-4

piperidine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(piperidin-1-yl)butyronitrile
4672-18-8

4-(piperidin-1-yl)butyronitrile

Conditions
ConditionsYield
In toluene at 55 - 80℃;98%
With potassium carbonate; potassium iodide In acetonitrile at 20℃; for 18h;
In toluene at 10 - 60℃;
In toluene at 55 - 80℃;
4-chloro-phenol
106-48-9

4-chloro-phenol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(4-chlorophenoxy)butanenitrile
501941-41-9

4-(4-chlorophenoxy)butanenitrile

Conditions
ConditionsYield
With potassium carbonate In acetone for 24h; Heating;98%
With potassium carbonate In acetone for 20h; Reflux;85%
1-(o-fluorophenyl)piperazine
1011-15-0

1-(o-fluorophenyl)piperazine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(4-(2-fluorophenyl)piperazin-1-yl)butyronitrile
883874-55-3

4-(4-(2-fluorophenyl)piperazin-1-yl)butyronitrile

Conditions
ConditionsYield
Stage #1: 1-(o-fluorophenyl)piperazine; 4-bromobutanenitrile With potassium carbonate In acetonitrile for 10h; Heating / reflux;
Stage #2: With hydrogenchloride In water; ethyl acetate
Stage #3: With ammonia In water pH=11;
98%
With potassium carbonate; potassium iodide In acetonitrile Heating / reflux;93%
With potassium carbonate; potassium iodide In acetonitrile for 8h; Heating;84%
With potassium carbonate; potassium iodide In acetonitrile Reflux;
6-benzyloxy-2-(4-hydroxyphenyl)-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene

6-benzyloxy-2-(4-hydroxyphenyl)-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

6-benzyloxy-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]-2-[4-(3-cyanopropyloxy)phenyl]benzo[b]thiophene

6-benzyloxy-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]-2-[4-(3-cyanopropyloxy)phenyl]benzo[b]thiophene

Conditions
ConditionsYield
With caesium carbonate In water; N,N-dimethyl-formamide98%
With caesium carbonate In water; N,N-dimethyl-formamide98%
1-(7-methoxy-1-naphthalenyl)piperazine
120991-78-8

1-(7-methoxy-1-naphthalenyl)piperazine

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-[4-(7-Methoxy-1-naphthyl)piperazino]butyronitrile

4-[4-(7-Methoxy-1-naphthyl)piperazino]butyronitrile

Conditions
ConditionsYield
98%
4-cyanophenol
767-00-0

4-cyanophenol

4-bromobutanenitrile
5332-06-9

4-bromobutanenitrile

4-(4-cyanophenoxy)butanenitrile

4-(4-cyanophenoxy)butanenitrile

Conditions
ConditionsYield
With potassium carbonate In acetone for 20h; Reflux;98%

5332-06-9Relevant articles and documents

A convenient and practical method for conversion of primary alkyl chlorides to highly pure bromides (≥99%)

Li,Singh,Labrie

, p. 733 - 743 (1994)

Repeated treatment (second after the aqueous work-up) of primary alkyl chlorides with ten equivalents (each) of lithium bromide in 3-pentanone at 120 °C for a total of five hours gave the corresponding bromides in excellent yield (86-96%) and with high chemical purity (≥99%).

SUBSTITUTED IMIDAZOLES FOR THE INHIBITION OF TGF-BETA AND METHODS OF TREATMENT

-

Paragraph 0042, (2020/03/15)

This disclosure relates to low molecular weight substituted imidazoles that inhibit the TGF-b signaling pathway. More specifically, this disclosure relates to methods of using said imidazoles for the treatment of diseases related to the TGF-b signaling pathways including, but not limited to, atherosclerosis, Marfan syndrome, Loeys-Dietz syndrome, obesity, diabetes, multiple sclerosis, keratoconus, idiopathic pulmonary fibrosis, Alzheimer's Disease, chronic kidney disease, and scleroderma.

C-substituted, 1H-azoles for amphoteric, solvent-less proton conductivity

-

, (2016/01/09)

Disclosed herein are the compounds shown below. Also disclosed are methods of making the compounds. R1=—O—; R2=any alkyl chain; R3=—CH3, —CN, —COOCH3, -tetrazole, -imidazole, or -triazole; R4=—H or —R5; R5=—H, -halogen, —C≡CH, or —C≡C—; n is a positive integer; and m is a positive integer.

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