80552-14-3

Basic information

• Product Name: 3-(4-chlorophenyl)-4-hydroxybutyric acid
• Synonyms: Benzenebutanoic acid, 4-chloro-gamma-hydroxy-
• CAS NO: 80552-14-3
• Molecular Formula: C10H11ClO3
• Molecular Weight: 0
• Mol File: 80552-14-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 398°C at 760 mmHg
• Flash Point: 194.5°C
• Appearance: /
• Density: 1.34g/cm³
• Vapor Pressure: 4.76E-07mmHg at 25°C
• Refractive Index: 1.577
• CAS DataBase Reference: 3-(4-chlorophenyl)-4-hydroxybutyric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-chlorophenyl)-4-hydroxybutyric acid(80552-14-3)
• EPA Substance Registry System: 3-(4-chlorophenyl)-4-hydroxybutyric acid(80552-14-3)

Safety Data

• Hazardous Substances Data: 80552-14-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H11ClO3/c11-8-3-1-7(2-4-8)9(12)5-6-10(13)14/h1-4,9,12H,5-6H2,(H,13,14)

Upstream product

• 99-91-2 para-chloroacetophenone 
• 29582-39-6 3-(4-chlorobenzoyl)acrylic acid 
• 3984-34-7 4-(4-chlorophenyl)-4-oxobutanoic acid 
• 108-30-5 succinic acid anhydride 
• 108-90-7 chlorobenzene 

Downstream Products

• 79559-98-1 [(1R,4R)-4-(4-Chloro-phenyl)-1,2,3,4-tetrahydro-naphthalen-1-yl]-methyl-amine; hydrochloride 

Relevant articles and documents

Photo-induced radical borylation of hemiacetals via C–C bond cleavage

In this study, we reported a photo-induced radical borylation of hemiacetal derivatives via C–C bond cleavage. This transformation can be realized under mild conditions with simple reaction settings and irradiation of visible light. A series of substrates, including both cyclic and linear hemiacetal derivatives, were effectively transformed to the borylation product in moderate to good yields. Finally, the mechanism was studied in detail by DFT calculations, suggesting insight of the radical borylation process.

A sertraline hydrochloride impurity preparation method (by machine translation)

The invention discloses a sertraline hydrochloride preparation method of impurities, in particular comprising a formula 6 by the Leuckart reaction to obtain a compound of the formula 7 compound, with the insulated hydrochloride salt obtained in the reaction formula 8 cis-isomer of the compound, wherein the formula 6 compound in the location of the chloropropyl substituted cyclohexanone substituted meta or para position. Preparation method of this invention is simple, high purity, obtained impurity can be used for qualitative and quantitative analysis, so as to improve the safety of medicine sertraline hydrochloride. (by machine translation)