3-(4-Chlorophenyl)glutaramic acid
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
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)
MSDS
- Language:English Provider:ALFA
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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3-(4-Chlorophenyl)glutaramic acid(1141-23-7)Related Product Information
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- 1,3-Acetonedicarboxylic acid
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- 3-(4-Chlorophenyl)glutaric acid
- Baclofen impurity 6
- BETA-(4-CHLOROPHENYL)GLUTARIC ANHYDRIDE
- Baclofen-d4
- 4-(4-Chlorophenyl)-2-pyrrolidinone
- 3-(4-CHLOROPHENYL) GLUTARIMIDE
- Baclofen Impurity 2 (beta-(4-Chlorophenyl)-gama-Hydroxybutyric Acid)
- Baclofen Impurity 3 (Mixture of Diastereomers)
- ETHYL 4-(4-CHLOROPHENYL)-1-(2-ETHOXY-2-OXOETHYL)-2-METHYL-6-OXO-1,4,5,6-TETRAHYDRO-3-PYRIDINECARBOXYLATE
- ETHYL 4-(2,4-DICHLOROPHENYL)-2-METHYL-6-OXO-1,4,5,6-TETRAHYDRO-3-PYRIDINECARBOXYLATE
- 3-(4-Chlorophenyl)glutaramic acid
- Chlorophenyl