39885-08-0

Basic information

• Product Name: (2-AMINO-6-CHLORO-PHENYL)-METHANOL
• Synonyms: (2-AMINO-6-CHLORO-PHENYL)-METHANOL;2-Amino-6-chlorobenzyl alcohol;2-Chloro-6-aminobenzyl alcohol;Benzenemethanol,2-amino-6-chloro-;2-Amino-6-chlorobenzenemethanol
• CAS NO: 39885-08-0
• Molecular Formula: C₇H₈ClNO
• Molecular Weight: 157.59752
• Mol File: 39885-08-0.mol
• Article Data: 24

Chemical Properties

• Melting Point: 76-78℃
• Boiling Point: 324.2°C at 760 mmHg
• Flash Point: 149.8°C
• Appearance: /
• Density: 1.341g/cm³
• Vapor Pressure: 0.000102mmHg at 25°C
• Refractive Index: 1.63
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 13.84±0.10(Predicted)
• CAS DataBase Reference: (2-AMINO-6-CHLORO-PHENYL)-METHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: (2-AMINO-6-CHLORO-PHENYL)-METHANOL(39885-08-0)
• EPA Substance Registry System: (2-AMINO-6-CHLORO-PHENYL)-METHANOL(39885-08-0)

Safety Data

• Hazardous Substances Data: 39885-08-0(Hazardous Substances Data)

Usage

General Description

(2-AMINO-6-CHLORO-PHENYL)-METHANOL is a chemical compound with the molecular formula C7H8ClNO. It is a derivative of phenol and contains an amino group and a chlorine atom. (2-AMINO-6-CHLORO-PHENYL)-METHANOL is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It has potential applications in drug discovery and development due to its unique structure and properties. Additionally, it is important in the field of organic chemistry for the preparation of various derivatives and building blocks for the synthesis of more complex molecules. Overall, (2-AMINO-6-CHLORO-PHENYL)-METHANOL plays a vital role in various chemical and pharmaceutical processes.

InChI:InChI=1/C7H8ClNO/c8-6-2-1-3-7(9)5(6)4-10/h1-3,10H,4,9H2

Upstream product

• 6575-11-7 2-amino-6-chlorobenzonitrile 
• 1404491-67-3 2-(3,5-dimethylphenyl)-5-isobutylquinoline 
• 67-63-0 isopropyl alcohol 
• 123-54-6 acetylacetone 
• 2148-56-3 2-chloro-6-aminobenzoic acid 

Downstream Products

• 1027961-10-9 4-(3-chloro-2-hydroxymethyl-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester 
• 852571-93-8 [2-chloro-6-(isopropylamino)phenyl]methanol 
• 35490-90-5 2-amino-6-chlorobenzaldehyde 
• 1404491-67-3 2-(3,5-dimethylphenyl)-5-isobutylquinoline 
• 1596243-33-2 5-chloro-2-phenylquinazoline 
• 945543-21-5 (2-chloro-6-iodophenyl)methanol 

Relevant articles and documents

Construction of a benzo[b]azepine skeleton through decarboxylative ylide [6+1] annulations with modified vinyl benzoxazinanones

A Lewis acid-promoted [6+1] annulation between sulfur ylides and modified vinyl benzoxazinanones was described. In this reaction, the newly designed vinyl benzoxazinanones could serve as a novel six-atom synthon, and the key to success is the installation of an electron-withdrawing group on the alkene moiety of the benzoxazinanones. A broad range of substrates are compatible with this mild reaction system, thereby providing a facile and practical approach for constructing a benzo[b]azepine skeleton.

IMIDAZOPIPERAZINONE INHIBITORS OF TRANSCRIPTION ACTIVATING PROTEINS

The present disclosure relates to heterocyclic compounds and methods which may be useful as inhibitors of transcription activating proteins such as CBP and P300 for the treatment or prevention of diseases such as proliferative diseases, inflammatory disorders, autoimmune diseases, and fibrotic diseases.

ORGANOMETALLIC COMPOUND, ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE ORGANOMETALLIC COMPOUND, AND DIAGNOSTIC COMPOSITION INCLUDING THE ORGANOMETALLIC COMPOUND

An organometallic compound represented by Formula 1, an organic light-emitting device including the organometallic compound, and a diagnostic composition including the organometallic compound. wherein, in Formula 1, R1 to R12 and R19 are the same as described in the specification.