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Benzenemethanamine, 2-chloro-N-(4-methylphenyl)-, also known as 2-chloro-N-(4-methylphenyl)benzenemethanamine, is an organic compound with the chemical formula C14H14ClN. It is a derivative of benzenemethanamine, featuring a chloro group at the 2-position and a 4-methylphenyl group attached to the nitrogen atom. Benzenemethanamine, 2-chloro-N-(4-methylphenyl)- is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is important to handle this substance with care due to its potential toxicity and reactivity.

7192-75-8

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7192-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7192-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7192-75:
(6*7)+(5*1)+(4*9)+(3*2)+(2*7)+(1*5)=108
108 % 10 = 8
So 7192-75-8 is a valid CAS Registry Number.

7192-75-8SDS

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 p-tolyl-(2-chloro-benzyl)-amine

1.2 Other means of identification

Product number -
Other names p-Tolyl-(2-chlor-benzyl)-amin

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:7192-75-8 SDS

7192-75-8Downstream Products

7192-75-8Relevant academic research and scientific papers

Application of a catalyst-free Domino Mannich/Friedel-Crafts alkylation reaction for the synthesis of novel tetrahydroquinolines of potential antitumor activity

Castillo, Juan-Carlos,Jiménez, Elizabeth,Portilla, Jaime,Insuasty, Braulio,Quiroga, Jairo,Moreno-Fuquen, Rodolfo,Kennedy, Alan R.,Abonia, Rodrigo

, p. 932 - 947 (2018/02/09)

A useful and efficient method to construct diversely substituted 1,2,3,4-tetrahydroquinolines in good to excellent yields has been developed through a catalyst-free Domino Mannich and intramolecular Friedel-Crafts alkylation reactions of N-arylamines with

Synthesis and reduction of nitrones of 2-chlorobenzaldehyde and their antifungal potential

Matharu, Balbir Kaur,Sharma,Manrao

, p. 917 - 918 (2007/10/03)

Condensation of 2-chlorobenzaldehyde with phenylhydroxylamines resulted in the foripation of C-(2-chlorophenyl)-N-phenylnitrones (1a-6a) which were characterized on the basis of elemental analysis and spectral studies. Sodium borohydride reduction of the nitrones was carried out and the nitrones were screened for their antifungal potential against five phytopathogenic fungi.

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