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53868-45-4

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53868-45-4 Usage

General Description

4-Benzoylbenzylamine hydrochloride, also known as 4'-Aminodiphenylmethane hydrochloride, is a chemical compound with a molecular formula C14H14ClN. It is a white to off-white crystalline powder that is soluble in water and ethanol. 4-Benzoylbenzylamine hydrochloride is commonly used as a building block in the synthesis of various pharmaceuticals and organic compounds. It is also used as a precursor in the production of dyes, pigments, and other industrial chemicals. 4-Benzoylbenzylamine hydrochloride has a wide range of applications in the pharmaceutical and chemical industries due to its versatile reactivity and stability.

Check Digit Verification of cas no

The CAS Registry Mumber 53868-45-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,6 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53868-45:
(7*5)+(6*3)+(5*8)+(4*6)+(3*8)+(2*4)+(1*5)=154
154 % 10 = 4
So 53868-45-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO.ClH/c15-10-11-6-8-13(9-7-11)14(16)12-4-2-1-3-5-12;/h1-9H,10,15H2;1H

53868-45-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-(Aminomethyl)phenyl)(phenyl)methanone hydrochloride?

1.2 Other means of identification

Product number -
Other names 4-methylphenyl malonaldehyde

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:53868-45-4 SDS

53868-45-4Upstream product

53868-45-4Relevant articles and documents

Electronic Effects of Aryl and Heteroaryl Groups on the Rate of Nucleophilic Displacement of Chlorine from 5-Heteroaryl(or Aryl)-2-chloropyrimidines by Piperidine

Allen, David W.,Buckland, David J.,Hutley, Barrie G.

, p. 463 - 467 (2007/10/02)

The kinetics of nucleophilic displacement of chlorine from a series of 2-chloro-5-heteroaryl(or aryl)pyrimidines by piperidine have been studied in order to assess the electronic effects of the 5-substituent.The observed order of reactivity is 5-(1-methyl

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