906811-49-2

Basic information

• Product Name: Benzenemethanol, 2-amino-3-fluoro- (9CI)
• Synonyms: Benzenemethanol, 2-amino-3-fluoro- (9CI);(2-aMino-3-fluorophenyl)Methanol;2-Amino-3-fluorobenzyl alcohol;BENZENEMETHANOL, 2-AMINO-3-FLUORO-
• CAS NO: 906811-49-2
• Molecular Formula: C₇H₈FNO
• Molecular Weight: 141.1429232
• Product Categories: VARIOUSAMINE
• Mol File: 906811-49-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 263.4±25.0 °C(Predicted)
• Appearance: /
• Density: 1.286±0.06 g/cm3(Predicted)
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 13.94±0.10(Predicted)
• CAS DataBase Reference: Benzenemethanol, 2-amino-3-fluoro- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-amino-3-fluoro- (9CI)(906811-49-2)
• EPA Substance Registry System: Benzenemethanol, 2-amino-3-fluoro- (9CI)(906811-49-2)

Safety Data

• Hazardous Substances Data: 906811-49-2(Hazardous Substances Data)

Usage

General Description

Benzenemethanol, 2-amino-3-fluoro- (9CI) is a chemical compound with the molecular formula C7H8FNO. It is a derivative of benzenemethanol with an amino group and a fluorine atom attached to the ring. Benzenemethanol, 2-amino-3-fluoro- (9CI) is commonly used in pharmaceutical research and drug development due to its potential biological activity and therapeutic applications. It is also used as a building block in the synthesis of various organic compounds. The exact properties and uses of the compound may vary depending on its specific application and chemical context.

Upstream product

• 144851-82-1 2-amino-3-fluoro-benzoic acid methyl ester 
• 825-22-9 3-fluoroanthranilic acid 

Downstream Products

• 854538-94-6 2-amino-3-fluorobenzaldehyde 

Relevant articles and documents

Enantioconvergent Amination of Racemic Tertiary C-H Bonds

Racemization is considered to be an intrinsic stereochemical feature of free radical chemistry as can be seen in traditional radical halogenation reactions of optically active tertiary C-H bonds. If the facile process of radical racemization could be effe

Catalytic Asymmetric [4 + 3] Annulation of C, N-Cyclic Azomethine Imines with Copper Allenylidenes

The first asymmetric decarboxylative [4 + 3] annulation of propargylic carbamates with C,N-cyclic azomethine imines has been developed successfully by a copper-N-heterocyclic carbine system. This strategy led to a series of optically active isoquinoline-f

HUMAN PLASMA KALLIKREIN INHIBITORS

Disclosed are compounds of formula (I), as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also provided are pharmaceutical compositions comprising at least one compound of the invention, and methods involving use of the compounds and compositions of the invention in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.