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

10398-99-9

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10398-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10398-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10398-99:
(7*1)+(6*0)+(5*3)+(4*9)+(3*8)+(2*9)+(1*9)=109
109 % 10 = 9
So 10398-99-9 is a valid CAS Registry Number.

10398-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzhydryliden-phenylsulfonamid

1.2 Other means of identification

Product number -
Other names N-Benzhydrylidene-benzenesulfonamide

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:10398-99-9 SDS

10398-99-9Downstream Products

10398-99-9Relevant academic research and scientific papers

5-(Diarylimino)- And 5-(sulfoximido)dibenzothiophenium triflates: syntheses and applications as electrophilic aminating reagents

Li, Zhen,Vijaykumar, Gonela,Li, Xiangdong,Golz, Christopher,Alcarazo, Manuel

, p. 2941 - 2948 (2021)

The one-pot synthesis of well-defined 5-(diarylimino) and 5-(sulfoximido)dibenzothiophenium triflates, respectively from diarylimines or sulfoximines, is reported and the structures of a series of these compounds are elucidated by X-ray crystallography. In analogy to their hypervalent I(iii) analogues, the iminoyl and sulfoximidoyl groups of these compounds can be selectively transferred to organic substrates. Specifically, the uncatalyzed imination of thiols or sulfinates proceeds with good yields, while under the mild reaction conditions offered by visible light photoredox catalysis, the radical amination of hydrazones or the sulfoximidation of benzylic, allylic and propargylic C-H bonds takes place satisfactorily.

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