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Benzenesulfonamide, 2-amino-N-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63132-70-7

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63132-70-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63132-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63132-70:
(7*6)+(6*3)+(5*1)+(4*3)+(3*2)+(2*7)+(1*0)=97
97 % 10 = 7
So 63132-70-7 is a valid CAS Registry Number.

63132-70-7SDS

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-amino-N-(4-chlorophenyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names Benzenesulfonamide,2-amino-N-(4-chlorophenyl)

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:63132-70-7 SDS

63132-70-7Relevant academic research and scientific papers

Transition-Metal-Free Tandem Cyclization/ N-Arylation Reaction: A Method to Access Biaryl Sultam Derivatives via a Diradical Pathway

Thorat, Vijaykumar H.,Hsieh, Jen-Chieh,Cheng, Chien-Hong

supporting information, p. 6623 - 6627 (2020/09/02)

A novel procedure for the transition-metal-free tandem cyclization/N-arylation reaction sequence of an aryne with a 1,2,3,4-benzothiatriazine-1,1-dioxide is reported. This reaction goes through the intramolecular homolytic cyclization to generate an N-H b

Dibenzo[1,2,5]thiadiazepines are non-competitive GABAA receptor antagonists

Ramirez-Martinez, Juan F.,Gonzalez-Chavez, Rodolfo,Guerrero-Alba, Raquel,Reyes-Gutierrez, Paul E.,Martinez, Roberto,Miranda-Morales, Marcela,Espinosa-Luna, Rosa,Gonzalez-Chavez, Marco M.,Barajas-Lopez, Carlos

, p. 894 - 913 (2013/03/28)

A new process for obtaining dibenzo[c,f][1,2,5]thiadiazepines (DBTDs) and their effects on GABAA receptors of guinea pig myenteric neurons are described. Synthesis of DBTD derivatives began with two commercial aromatic compounds. An azide group was obtain

Benzothiadiazine compounds, and pharmaceutical composition comprising the same

-

, (2008/06/13)

A compound of the formula: STR1 wherein R' is phenyl, phenyl which is substituted with halogen, lower alkyl, lower alkoxy, halo lower alkyl, lower alkylamino, lower alkylthio, phenoxy, carboxy, lower alkoxycarbonyl, carboxy lower alkyl, lower alkoxycarbon

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