149947-16-0

Basic information

• Product Name: 1-Bromo-3-bromomethyl-2-fluorobenzene
• Synonyms: 1-Bromo-3-bromomethyl-2-fluorobenzene
• CAS NO: 149947-16-0
• Molecular Formula: C₇H₅Br₂F
• Molecular Weight: 267.93
• Mol File: 149947-16-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 60℃/0.1mm
• Flash Point: 107.9°C
• Appearance: /
• Density: 1.923g/cm³
• Vapor Pressure: 0.0271mmHg at 25°C
• Refractive Index: 1.583
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1-Bromo-3-bromomethyl-2-fluorobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-3-bromomethyl-2-fluorobenzene(149947-16-0)
• EPA Substance Registry System: 1-Bromo-3-bromomethyl-2-fluorobenzene(149947-16-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 149947-16-0(Hazardous Substances Data)

Usage

Uses

Used to obtain the target inhibitors. A new quasi-one-dimensional molecular solid based on Ni (mnt) 2 anion: Crystal structure and spin-gap transition 4-Bromo-2-fluorobenzyl bromide acts as stasrting material.

InChI:InChI=1/C7H5Br2F/c8-4-5-2-1-3-6(9)7(5)10/h1-3H,4H2

Upstream product

• 1072-85-1 o-fluorobromobenzene 
• 261723-32-4 1-bromo-2-fluoro-3-(hydroxymethyl)benzene 
• 59907-12-9 3-bromo-2-fluorotoluene 
• 161957-56-8 3-bromo-2-fluorobenzoic acid 

Downstream Products

• 447463-24-3 (3-{4-[1-(3-bromo-2-fluoro-benzyloxy)-ethyl]-2-methoxy-5-nitro-phenoxy}-propyl)-carbamic acid tert-butyl ester 
• 149947-15-9 3-bromo-2-fluorobenzaldehyde 
• 947251-11-8 C₂₉H₃₈F₂N₂O₆ 
• 947251-00-5 C₃₀H₄₀F₂N₂O₆ 
• 887969-60-0 C₁₆H₂₁BrFNO₄ 

Relevant articles and documents

Ansa-Zirconocene Catalysts for Isotactic-Selective Propene Polymerization at High Temperature: A Long Story Finds a Happy Ending

Absolute rigidity is rare in the "soft"world of organometallics. Here we introduce two cyclopenta[a]triptycyl ansa-zirconocene catalysts for isotactic-selective propene polymerization, designed by means of an integrated high-throughput experimentation/qua

Nitrile in the Hole: Discovery of a Small Auxiliary Pocket in Neuronal Nitric Oxide Synthase Leading to the Development of Potent and Selective 2-Aminoquinoline Inhibitors

Neuronal nitric oxide synthase (nNOS) inhibition is a promising strategy to treat neurodegenerative disorders, but the development of nNOS inhibitors is often hindered by poor pharmacokinetics. We previously developed a class of membrane-permeable 2-amino

OXO-HETEROCYCLIC SUBSTITUTED CARBOXYLIC ACID DERIVATIVES AND THE USE THEREOF

The present application relates to novel carboxylic acid derivatives having an oxo-substituted azaheterocyclic partial structure, processes for their preparation, their use for the treatment and/or prophylaxis of diseases, and their use for producing medicaments for the treatment and/or prophylaxis of diseases, especially for the treatment and/or prevention of cardiovascular disorders.