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4-FLUORO-2-METHYLBENZYL BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862539-91-1

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862539-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862539-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,5,3 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 862539-91:
(8*8)+(7*6)+(6*2)+(5*5)+(4*3)+(3*9)+(2*9)+(1*1)=201
201 % 10 = 1
So 862539-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BrF/c1-6-4-8(10)3-2-7(6)5-9/h2-4H,5H2,1H3

862539-91-1 Well-known Company Product Price

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  • CAS number
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  • Alfa Aesar

  • (H26849)  4-Fluoro-2-methylbenzyl bromide, 97%   

  • 862539-91-1

  • 1g

  • 1469.0CNY

  • Detail

  • Alfa Aesar

  • (H26849)  4-Fluoro-2-methylbenzyl bromide, 97%   

  • 862539-91-1

  • 5g

  • 4524.0CNY

  • Detail

862539-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Bromomethyl)-4-fluoro-2-methylbenzene

1.2 Other means of identification

Product number -
Other names 1-(bromomethyl)-4-fluoro-2-methylbenzene

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:862539-91-1 SDS

862539-91-1Downstream Products

862539-91-1Relevant academic research and scientific papers

Catalytic Asymmetric (3 + 3) Cycloaddition of Oxyallyl Zwitterions with α-Diazomethylphosphonates

Liu, Yan,Peng, Xian,Peng, Yungui,She, Rui,Zhou, Xin

, p. 7295 - 7300 (2021/10/01)

The unique structure of oxyallyls represents a significant challenge for their catalytic asymmetric applications. Herein, an unprecedented chiral imidodiphosphoric acid-catalytic enantioselective (3 + 3) cycloaddition between oxyallyl zwitterions generate

PYRROLOY2,3-c¨PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE

-

Page/Page column 46, (2010/11/27)

Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.

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