ChemicalBook--->CAS DataBase List--->4619-18-5

4619-18-5

4619-18-5 Structure

4619-18-5 Structure
IdentificationBack Directory
[Name]

4-(4-Chlorophenyl)butanic acid
[CAS]

4619-18-5
[Synonyms]

4-Chlorobenzenebutanoic acid
-(4-Chlorophenyl)butanic acid
4-(4-Chlorophenyl)butanic acid
Benzenebutanoic acid, 4-chloro-
4-(4-CHLORO-PHENYL)-BUTYRIC ACID
4-(4-chlorophenyl)butanoic acid(SALTDATA: FREE)
[Molecular Formula]

C10H11ClO2
[MDL Number]

MFCD06810494
[MOL File]

4619-18-5.mol
[Molecular Weight]

198.65
Chemical PropertiesBack Directory
[Melting point ]

55 °C
[Boiling point ]

181-184 °C
[density ]

1.227±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.74±0.10(Predicted)
[Appearance]

White to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H318-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P280-P305+P351+P338-P310
[HS Code ]

29163990
Spectrum DetailBack Directory
[Spectrum Detail]

4-(4-Chlorophenyl)butanoic acid(4619-18-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-(4-Chlorobenzoyl)propionic acid

3984-34-7

4-(4-Chlorophenyl)butanoic acid

4619-18-5

General procedure for the synthesis of 4-(4-chlorophenyl)butyric acid from 3-(4-chlorobenzoyl)propionic acid: A mixture of 4-(4-chlorophenyl)-4-oxobutanoic acid (1 eq.), potassium hydroxide (KOH, 3 eq.), and hydrazine hydrate (2.2 eq.) in ethylene glycol was placed in a reaction flask and azeotropically refluxed for 5 hr at 120-130 °C. Subsequently, the reaction temperature was gradually increased to 180 °C and the reflux was continued at 190 °C for 3 hours. After completion of the reaction, the reaction mixture was cooled to 25 °C, diluted with water and poured into 2.5 N hydrochloric acid (HCl) solution for acidification, and white crystals were precipitated to give 4-(4-chlorophenyl)butyric acid in 89% yield.

[References]

[1] Patent: US6410585, 2002, B1
[2] Journal of Medicinal Chemistry, 1982, vol. 25, # 8, p. 947 - 952
[3] Patent: US2005/165004, 2005, A1. Location in patent: Page/Page column 28
[4] Patent: WO2015/134973, 2015, A1. Location in patent: Page/Page column 97; 98
[5] Angewandte Chemie - International Edition, 2017, vol. 56, # 41, p. 12476 - 12480
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