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886762-70-5

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886762-70-5 Usage

Chemical Properties

light yellow crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 886762-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,7,6 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 886762-70:
(8*8)+(7*8)+(6*6)+(5*7)+(4*6)+(3*2)+(2*7)+(1*0)=235
235 % 10 = 5
So 886762-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrFNO2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H

886762-70-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Bromo-3-fluoro-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2-fluoro-6-bromonitrobenzene

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:886762-70-5 SDS

886762-70-5Relevant articles and documents

Design of two new chemotypes for inhibiting the Janus kinase 2 by scaffold morphing

Furet, Pascal,Gerspacher, Marc,Pissot-Soldermann, Carole

supporting information; scheme or table, p. 1858 - 1860 (2010/07/04)

JAK2 is a target of high interest in chronic myeloproliferative disorders drug research. Starting from a screening hit, two new JAK2 inhibitor chemotypes were designed by scaffold morphing. The prototype compounds of these new series showed nanomolar inhi

Synthesis of pyrrolnitrin and related halogenated phenylpyrroles

Morrison, Matthew D.,Hanthorn, Jason J.,Pratt, Derek A.

supporting information; experimental part, p. 1051 - 1054 (2009/07/18)

A general approach to halogenated arylpyrroles, including the antifungal natural product pyrrolnitrin, is described using newly synthesized halogenated pyrroles and 2,6-disubstituted nitrobenzenes or 2,6-disubstituted anilines.

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