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13711-29-0

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13711-29-0 Usage

General Description

2,3-Dichloro-5-methylaniline is a chemical compound with the molecular formula C7H7Cl2N. It is an aromatic amine that is commonly used in the production of dyes and pigments. 2,3-Dichloro-5-methylaniline is a derivative of aniline, with two chlorine atoms and a methyl group attached to the aromatic ring. 2,3-Dichloro-5-methylaniline is known to be toxic and can cause irritation to the skin, eyes, and respiratory system upon exposure. It is important to handle and store this chemical with proper safety precautions to avoid any potential health hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 13711-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,1 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13711-29:
(7*1)+(6*3)+(5*7)+(4*1)+(3*1)+(2*2)+(1*9)=80
80 % 10 = 0
So 13711-29-0 is a valid CAS Registry Number.

13711-29-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dichloro-5-methylaniline

1.2 Other means of identification

Product number -
Other names 2,3-DICHLORO-5-METHYLBENZENAMINE

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:13711-29-0 SDS

13711-29-0Relevant articles and documents

3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands

Szymanska, Ewa,Pickering, Darryl S.,Nielsen, Birgitte,Johansen, Tommy N.

, p. 6390 - 6401 (2011/03/17)

On the basis of X-ray structures of ionotropic glutamate receptor constructs in complex with amino acid-based AMPA and kainate receptor antagonists, a series of rigid as well as flexible biaromatic alanine derivatives carrying selected hydrogen bond acceptors and donors have been synthesized in order to investigate the structural determinants for receptor selectivity between AMPA and the GluR5 subtype of kainate receptors. Compounds selective for either GluR5 or AMPA receptors were identified. One particular substituent position appeared to be of special importance for control of ligand selectivity. Using molecular modeling the observed structure-activity relationships at AMPA and GluR5 receptors were deduced.

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