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4'-Amino-2-chlorobenzophenone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62261-41-0

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62261-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62261-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,6 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62261-41:
(7*6)+(6*2)+(5*2)+(4*6)+(3*1)+(2*4)+(1*1)=100
100 % 10 = 0
So 62261-41-0 is a valid CAS Registry Number.

62261-41-0SDS

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 (4-aminophenyl)-(2-chlorophenyl)methanone

1.2 Other means of identification

Product number -
Other names 4'-amino-2-chloro-benzophenone

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:62261-41-0 SDS

62261-41-0Downstream Products

62261-41-0Relevant academic research and scientific papers

AGRICULTURAL CHEMICALS

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Page/Page column 101, (2019/08/08)

The present invention relates to picolinic acid derivatives that are useful in treating fungal diseases ofplants.

Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline

Xu, Qian,Yu, Gang,Liu, Min,Peng, Chang,Banks, M. Katherine,Xu, Weijian,Wu, Ruoxi,Lu, Yanbing

, p. 5133 - 5136 (2018/10/24)

This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.

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