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2,3-DICHLOROBENZYL BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57915-78-3

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57915-78-3 Usage

Chemical Properties

White low melting solid

Check Digit Verification of cas no

The CAS Registry Mumber 57915-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,1 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57915-78:
(7*5)+(6*7)+(5*9)+(4*1)+(3*5)+(2*7)+(1*8)=163
163 % 10 = 3
So 57915-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BrCl2/c8-4-5-2-1-3-6(9)7(5)10/h1-3H,4H2

57915-78-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Bromomethyl)-2,3-dichlorobenzene

1.2 Other means of identification

Product number -
Other names 1-(bromomethyl)-2,3-dichlorobenzene

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:57915-78-3 SDS

57915-78-3Relevant academic research and scientific papers

Pyrazolopyrimidine derivatives as PI3 kinase inhibitors

-

, (2015/09/22)

PI3Kβ selective compounds having the structure

PYRAZOLOPYRIMIDINE DERIVATIVES AS PI3 KINASE INHIBITORS

-

, (2013/03/26)

The present invention relates to compounds of formula (I) in which R1, R2, R3 and n have the meaning given in the specification and also relates to the use of these pyrazolopyrimidine derivatives for the modulation, notably the inhibition of the activity or function of the phosphoinositide 3'OΗ kinase family (hereinafter PI3 kinases), wherein the compounds of formula (I) are described as selective inhibitors of PI3K[beta] activity.

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