851335-09-6

Basic information

• Product Name: 4-CARBOXY-2-CHLOROPHENYLBORONIC ACID
• Synonyms: 4-BORONO-3-CHLOROBENZOIC ACID;(4-CARBOXY-2-CHLORO)BENZENEBORONIC ACID;4-CARBOXY-2-CHLOROPHENYLBORONIC ACID;2-CHLORO-4-CARBOXYPHENYLBORONIC ACID;4-Carboxy-2-Chlorophenylboroni;4-Carboxy-2-chlorobenzeneboronic acid 97%;2-chloro-4-carboxylphenylboronic acid;REF DUPL: 4-Carboxy-2-chlorophenylboronic acid
• CAS NO: 851335-09-6
• Molecular Formula: C₇H₆BClO₄
• Molecular Weight: 200.38
• Product Categories: blocks;BoronicAcids;Carboxes;Heterocyclic Compounds
• Mol File: 851335-09-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 208-210
• Boiling Point: 429.7 ºC at 760 mmHg
• Flash Point: 213.7 ºC
• Appearance: /
• Density: 1.55 g/cm³
• Vapor Pressure: 3.79E-08mmHg at 25°C
• Refractive Index: 1.603
• Storage Temp.: Keep Cold
• PKA: 3.71±0.10(Predicted)
• CAS DataBase Reference: 4-CARBOXY-2-CHLOROPHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CARBOXY-2-CHLOROPHENYLBORONIC ACID(851335-09-6)
• EPA Substance Registry System: 4-CARBOXY-2-CHLOROPHENYLBORONIC ACID(851335-09-6)

Safety Data

• Hazard Codes: Xi
• Statements: 41
• Safety Statements: 26-39
• HazardClass: IRRITANT, KEEP COLD
• Hazardous Substances Data: 851335-09-6(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 851335-09-6 differently. You can refer to the following data:
1. suzuki reaction
2. Reactant in the synthesis and characterization1, 3, 4-oxadiazole.

InChI:InChI=1/C7H6BClO4/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,12-13H,(H,10,11)

Relevant articles and documents

AMINO ALCOHOL DERIVATIVE, MEDICINAL COMPOSITION CONTAINING THE SAME, AND USE OF THESE

The present invention provides compounds represented by general formula (I): a prodrug thereof, or pharmaceutical acceptable salts thereof, wherein R1 is hydrogen or lower alkyl; each of R2 and R3 is independently hydrogen or lower alkyl; each of R4, R5 and R6 is independently hydrogen, halogen, lower alkyl or lower alkoxy; R7 is hydrogen or lower alkyl; R8 is hydrogen, halogen, lower alkyl, lower alkoxy, etc; R9 is -COR10, -A1-COR10, -O-A2-COR10, etc; Ar is optionally substituted phenyl or heteroaryl; and A is a bond, -OCH2-, etc, which exhibit potent and selective β3-adrenoceptor stimulating activities. The present invention also provides pharmaceutical compositions containing said compound, and uses thereof.