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352535-04-7

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352535-04-7 Usage

General Description

(S)-1,2,2-Triphenylethylamine is a chemical compound that belongs to the class of alkylamines. It is an organic compound with a molecular formula C20H19N and a molecular weight of 277.37 g/mol. The compound consists of a central amine group bonded to a triphenylethyl moiety, which contains three phenyl groups. (S)-1,2,2-Triphenylethylamine is commonly used in organic synthesis and as a chiral auxiliary in asymmetric synthesis. It is also used in pharmaceutical research and as a ligand in coordination chemistry. The compound has a white to off-white crystalline appearance and is typically handled and stored under dry and inert conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 352535-04-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 352535-04:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*0)+(1*4)=127
127 % 10 = 7
So 352535-04-7 is a valid CAS Registry Number.

352535-04-7 Well-known Company Product Price

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  • Aldrich

  • (553220)  (S)-(−)-1,2,2-Triphenylethylamine  97%

  • 352535-04-7

  • 553220-500MG

  • 2,389.14CNY

  • Detail

352535-04-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S)-1,2,2-triphenylethanamine

1.2 Other means of identification

Product number -
Other names Benzeneethanamine,a,b-diphenyl-,(aS)

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:352535-04-7 SDS

352535-04-7Downstream Products

352535-04-7Relevant articles and documents

Electrochemical Aziridination by Alkene Activation Using a Sulfamate as the Nitrogen Source

Li, Jin,Huang, Wenhao,Chen, Jingzhi,He, Lingfeng,Cheng, Xu,Li, Guigen

, p. 5695 - 5698 (2018)

The first direct aziridination of triaryl-substituted alkenes was achieved by means of an electrochemical process that could extend to multisubstituted styrenes. Specifically, hexafluoroisopropanol sulfamate was used as a nucleophilic nitrogen source. Mechanistic experiments suggest that this electrochemical process proceeds by stepwise formation of two C?N bonds through reactions between cationic carbon species and the sulfamate.

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