706786-42-7

Basic information

• Product Name: 3,5-DIFLUORO-4-METHOXYBENZYL BROMIDE
• Synonyms: 3,5-DIFLUORO-4-METHOXYBENZYL BROMIDE;4-(Bromomethyl)-2,6-difluoroanisole;4-(Bromomethyl)-2,6-difluoroanisole, 4-(Bromomethyl)-2,6-difluorophenyl methyl ether, 5-(Bromomethyl)-1,3-difluoro-2-methoxybenzene;5-(Bromomethyl)-1,3-difluoro-2-methoxybenzene
• CAS NO: 706786-42-7
• Molecular Formula: C8H7BrF2O
• Molecular Weight: 237.04
• Mol File: 706786-42-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 39-42℃
• Boiling Point: 242.0±35.0 °C(Predicted)
• Appearance: /
• Density: 1.566±0.06 g/cm3(Predicted)
• Water Solubility: Insoluble in water.
• CAS DataBase Reference: 3,5-DIFLUORO-4-METHOXYBENZYL BROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIFLUORO-4-METHOXYBENZYL BROMIDE(706786-42-7)
• EPA Substance Registry System: 3,5-DIFLUORO-4-METHOXYBENZYL BROMIDE(706786-42-7)

Safety Data

• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 706786-42-7(Hazardous Substances Data)

Usage

Description

3,5-Difluoro-4-methoxybenzyl bromide is an organic compound characterized by the presence of two fluorine atoms at the 3rd and 5th positions, a methoxy group at the 4th position, and a benzyl bromide functional group. This unique molecular structure endows it with specific chemical properties, making it a valuable compound in various applications.

Uses

Used in Research Applications:
3,5-Difluoro-4-methoxybenzyl bromide is used as a research chemical for studying its properties and potential applications in various fields. Its unique structure allows researchers to explore its reactivity, stability, and interactions with other molecules, which can lead to the development of new chemical processes and compounds.
Used in Organic Synthesis:
3,5-Difluoro-4-methoxybenzyl bromide serves as an intermediate in organic synthesis, where it can be used to produce a variety of complex organic molecules. Its presence of fluorine atoms and the methoxy group can impart specific characteristics to the final products, making it a versatile building block for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

Upstream product

• 706786-41-6 (3,5-difluoro-4-methoxy-phenyl)-methanol 
• 654-11-5 3,5-Difluoro-4-methoxybenzaldehyde 

Relevant articles and documents

PHARMACEUTICAL COMPOSITION COMPRISING A PYRAZOLE-O-GLUCOSIDE DERIVATIVE

The invention relates toa pharmaceutical composition comprising a pyrazole-O-glucoside derivative selected from the group of compounds (1) to (29) according to claim 1 in combination with at least one second therapeutic agent which is suitable in the trea

Analysis of the role of the active site tyrosine in human glutathione transferase A1-1 by unnatural amino acid mutagenesis

-