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1141-23-7

1141-23-7 Structure

1141-23-7 Structure
IdentificationMore
[Name]

3-(4-Chlorophenyl)glutaramic acid
[CAS]

1141-23-7
[Synonyms]

3-(4-CHLOROPHENYL)GLUTARAMIC ACID
3-(4-CHLOROPHENYL)GLUTARIC ACID MONOAMIDE
B-(4-CHLOROPHENYL) GLUTARIC ACID MONOAMIDE
-(4-Chlorophenyl)glutaricacidmonoamide
beta-(4-Chlorophenyl)glutaric acid monoamide
3-(4-Chlorophenyl)Glutaramic Acid Monoamide
[EINECS(EC#)]

917-377-0
[Molecular Formula]

C11H12ClNO3
[MDL Number]

MFCD00190251
[Molecular Weight]

241.67
[MOL File]

1141-23-7.mol
Chemical PropertiesBack Directory
[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)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
Hazard InformationBack Directory
[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]

3-(4-CHLOROPHENYL) GLUTARIMIDE

84803-46-3

3-(4-Chlorophenyl)glutaramic acid

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
Spectrum DetailBack Directory
[Spectrum Detail]

3-(4-Chlorophenyl)glutaramic acid(1141-23-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-(4-Chlorophenyl)glutaramic acid, 97%(1141-23-7)
[Sigma Aldrich]

1141-23-7(sigmaaldrich)
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