Basic information Safety Supplier Related

3-(4-Chlorophenyl)glutaramic acid

Basic information Safety Supplier Related

3-(4-Chlorophenyl)glutaramic acid Basic information

Product Name:
3-(4-Chlorophenyl)glutaramic acid
Synonyms:
  • -(4-Chlorophenyl)glutaricacidmonoamide
  • B-(4-CHLOROPHENYL) GLUTARIC ACID MONOAMIDE
  • 3-(4-CHLOROPHENYL)GLUTARAMIC ACID
  • 3-(4-CHLOROPHENYL)GLUTARIC ACID MONOAMIDE
  • beta-(4-Chlorophenyl)glutaric acid monoamide
  • 3-(4-Chlorophenyl)Glutaramic Acid Monoamide
  • Benzenepropanoic acid, b-(2-aMino-2-oxoethyl)-4-chloro-
  • 3-(p-chlorophenyl)glutaramic acid
CAS:
1141-23-7
MF:
C11H12ClNO3
MW:
241.67
EINECS:
917-377-0
Product Categories:
  • Organic acids
Mol File:
1141-23-7.mol
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3-(4-Chlorophenyl)glutaramic acid Chemical Properties

Melting point:
168-170°C
Boiling point:
494.9±40.0 °C(Predicted)
Density 
1.343±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Methanol (Slightly)
form 
Solid
pka
4.50±0.10(Predicted)
color 
White
BRN 
2460842
CAS DataBase Reference
1141-23-7(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36

MSDS

  • Language:English Provider:ALFA
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3-(4-Chlorophenyl)glutaramic acid Usage And Synthesis

Uses

3-(4-Chlorophenyl)glutaramic acids serves as a reagent for the synthesis of heterocyclic compounds as mGlu5 antagonists for treating urinary tract disorders, migraine, and gastroesophageal reflux disease.

Synthesis

84803-46-3

1141-23-7

General procedure for the synthesis of 3-(4-chlorophenyl)glutaric acid monoamide from 3-(4-chlorophenyl)glutaric acid monoamide: Intermediate IV (120 g, 0.537 mol) was taken, aqueous sodium hydroxide solution (600 μl, 15N) was added, and the reaction was stirred for 1.5 hr at 65-70 °C. After the reaction was completed, it was cooled to room temperature and toluene (500 ml) and deionized water (700 ml) were added. The mixture was stirred for 20 min, and the organic layer was discarded after standing and layering. The pH of the aqueous layer was adjusted to 2~3 with concentrated hydrochloric acid, left to stand and filtered, and the solids were washed with water. The solid was dried under vacuum at 55~60°C for 5 hours to give 116 g of white solid intermediate V in 89.5% yield.

References

[1] Patent: CN106187794, 2016, A. Location in patent: Paragraph 0025; 0030

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