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6307-78-4

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6307-78-4 Usage

General Description

2,6-dimethyl-3-nitrobenzoyl chloride is a chemical compound with the molecular formula C9H8ClNO4. It is derived from benzoyl chloride and contains a nitro group and two methyl groups attached to the benzene ring. 2,6-dimethyl-3-nitrobenzoyl chloride is primarily used as a reagent in organic synthesis, particularly in the preparation of pharmaceuticals and other organic compounds. It is also a key intermediate in the synthesis of various chemicals, including dyes, pigments, and agricultural products. The compound is a powerful acylating agent, which makes it useful in the modification of organic molecules. Additionally, it is important to handle this compound with care as it can be toxic and irritating to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 6307-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6307-78:
(6*6)+(5*3)+(4*0)+(3*7)+(2*7)+(1*8)=94
94 % 10 = 4
So 6307-78-4 is a valid CAS Registry Number.

6307-78-4SDS

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 2,6-dimethyl-3-nitrobenzoyl chloride

1.2 Other means of identification

Product number -
Other names 3-Nitro-2,6-dimethyl-benzoylchlorid

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:6307-78-4 SDS

6307-78-4Downstream Products

6307-78-4Relevant articles and documents

Structure-guided design of aminopyrimidine amides as potent, selective inhibitors of lymphocyte specific kinase: Synthesis, structure-activity relationships, and inhibition of in vivo T cell activation

DiMauro, Erin F.,Newcomb, John,Nunes, Joseph J.,Bemis, Jean E.,Boucher, Christina,Chai, Lilly,Chaffee, Stuart C.,Deak, Holly L.,Epstein, Linda F.,Faust, Ted,Gallant, Paul,Gore, Anu,Gu, Yan,Henkle, Brad,Hsieh, Faye,Huang, Xin,Kim, Joseph L.,Lee, Josie H.,Martin, Matthew W.,McGowan, David C.,Metz, Daniela,Mohn, Deanna,Morgenstern, Kurt A.,Oliveira-Dos-Santos, Antonio,Patel, Vinod F.,Powers, David,Rose, Paul E.,Schneider, Stephen,Tomlinson, Susan A.,Tudor, Yan-Yan,Turci, Susan M.,Welcher, Andrew,Zhao, Huilin,Zhu, Li,Zhu, Xiaotian

, p. 1681 - 1694 (2008/12/20)

The lymphocyte-specific kinase (Lck), a member of the Src family of cytoplasmic tyrosine kinases, is expressed in T cells and natural killer (NK) cells. Genetic evidence, including knockout mice and human mutations, demonstrates that Lck kinase activity i

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