66916-97-0

Basic information

• Product Name: 2-Bromo-4-methoxybenzyl Chloride (+ regioisomers)
• Synonyms: 2-Bromo-1-(chloromethyl)-4-methoxy-benzene;2-Bromo-4-methoxybenzyl Chloride (+ regioisomers);3-Bromo-4-(chloromethyl)-anisole;2-Bromo-4-methoxybenzyl Chloride 75% (+ regioisomers)
• CAS NO: 66916-97-0
• Molecular Formula: C₈H₈BrClO
• Molecular Weight: 235.51
• Product Categories: Aromatics Compounds;Aromatics
• Mol File: 66916-97-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer
• Solubility: Acetone, Dichloromethane, Ethyl Acetate
• CAS DataBase Reference: 2-Bromo-4-methoxybenzyl Chloride (+ regioisomers)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-4-methoxybenzyl Chloride (+ regioisomers)(66916-97-0)
• EPA Substance Registry System: 2-Bromo-4-methoxybenzyl Chloride (+ regioisomers)(66916-97-0)

Safety Data

• Hazardous Substances Data: 66916-97-0(Hazardous Substances Data)

Usage

Chemical Properties

Colorless Oil

Uses

This compound contains up to 25% of the two other regioisiomers.

Upstream product

• 50-00-0 formaldehyd 
• 2398-37-0 3-methoxyphenyl bromide 

Downstream Products

• 66916-98-1 2-(2-bromo-4-methoxyphenyl)acetonitrile 
• 54788-18-0 2-bromo-1-(bromomethyl)-4-methoxybenzene 
• 403482-37-1 3-(2-bromo-4-methoxyphenyl)-2,2-dimethylpropanal 
• 2059-80-5 <2-Brom-4-methoxy-benzyl>-cyan-essigsaeure 
• 120579-66-0 [2-(2-cyclohexyliden-ethyl)-cyclohex-1-enylmethyl]-trimethyl-ammonium; iodide 
• 111443-78-8 [2-(2-cyclohexyliden-ethyl)-4-methoxy-benzyl]-dimethyl-amine 
• 823816-91-7 cyclohexylidene-((E)-2-methylene-cyclohexyliden)-ethane 
• 99177-37-4 1-(2-bromo-4-methoxyphenyl)-N,N-dimethylmethanamine 
• 147085-55-0 2-<(2-bromo-4-methoxyphenyl)methyl>cyclohexanone 

Relevant articles and documents

HOMOALLYLAMINES AS FORMALDEHYDE-RESPONSIVE TRIGGERS

Probes for formaldehyde (FA) including a homoallylamine trigger group attached to a detectable moiety are provided. Aspects of the probes include luminogenic or fluorogenic probes, such as a probe including a quencher in energy-receiving proximity to a fl

Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.