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2,3-Difluoro-6-methoxybenzyl bromide, with the molecular formula C8H7BrF2O, is a colorless liquid chemical compound. It is derived from benzyl bromide and features both methoxy and difluoro functional groups. This versatile building block in organic synthesis is known for its reactivity and stability, making it a valuable tool for chemical research and industrial applications. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, playing a crucial role in the development of new drugs and agrochemicals.

886501-83-3

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886501-83-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Difluoro-6-methoxybenzyl bromide is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique functional groups and reactivity allow for the creation of a wide range of medicinal compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical field, 2,3-difluoro-6-methoxybenzyl bromide is utilized as a starting material for the production of various agrochemicals. Its properties make it suitable for the synthesis of compounds that can be used in pest control, crop protection, and other agricultural applications, contributing to increased crop yields and more effective pest management.
Used in Organic Synthesis:
2,3-Difluoro-6-methoxybenzyl bromide is employed as a versatile building block in organic synthesis. Its methoxy and difluoro functional groups provide a foundation for the creation of a diverse array of organic compounds, which can be further modified and used in various chemical and industrial processes.
Used in Chemical Research:
As a valuable tool in chemical research, 2,3-difluoro-6-methoxybenzyl bromide is used to explore new reaction pathways, develop innovative synthetic methods, and study the properties of related compounds. Its stability and reactivity make it an ideal candidate for probing the limits of chemical reactions and understanding the underlying mechanisms at play.

Check Digit Verification of cas no

The CAS Registry Mumber 886501-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,0 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 886501-83:
(8*8)+(7*8)+(6*6)+(5*5)+(4*0)+(3*1)+(2*8)+(1*3)=203
203 % 10 = 3
So 886501-83-3 is a valid CAS Registry Number.

886501-83-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H26380)  2,3-Difluoro-6-methoxybenzyl bromide, 97%   

  • 886501-83-3

  • 1g

  • 689.0CNY

  • Detail
  • Alfa Aesar

  • (H26380)  2,3-Difluoro-6-methoxybenzyl bromide, 97%   

  • 886501-83-3

  • 5g

  • 2292.0CNY

  • Detail

886501-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Difluoro-6-methoxybenzyl bromide

1.2 Other means of identification

Product number -
Other names 3-(bromomethyl)-1,2-difluoro-4-methoxybenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:886501-83-3 SDS

886501-83-3Upstream product

886501-83-3Relevant academic research and scientific papers

NITROGENATED FUSED RING DERIVATIVE, PHARMACEUTICAL COMPOSITION COMPRISING THE SAME, AND USE OF THE SAME FOR MEDICAL PURPOSES

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Page/Page column 30, (2010/01/29)

[Purpose] The present invention provides compounds useful as agents for the prevention or treatment of a sex hormone-dependent disease or the like. [Solution] The present invention provides nitrogen-containing fused ring derivatives represented by the following general formula (I) which has a GnRH antagonistic activity, prodrugs, salts, pharmaceutical compositions containing the same, medicinal uses thereof and the like. In the formula (I), rings A and B are independently aryl or heteroaryl; RA and RB are independently halogen, cyano, alkyl, alkylsulfonyl, -OW1, -SW1, -COW2, -NW3W4, -SO2NW3W4, aryl, etc.; RC is H or alkyl; E is oxygen atom, etc.; U is single bond or alkylene; and X is Y, -CO-Y, -SO2-Y -S-(alkylene)-Y, -O-(alkylene)-Y, -SO2-(alkylene)-Y, etc.; Y is Z or amino, etc.; and Z is cycloalkyl, heterocycloalkyl, aryl, heteroaryl, etc.

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