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6971-74-0

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6971-74-0 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 35, p. 123, 1970 DOI: 10.1021/jo00826a027

Check Digit Verification of cas no

The CAS Registry Mumber 6971-74-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6971-74:
(6*6)+(5*9)+(4*7)+(3*1)+(2*7)+(1*4)=130
130 % 10 = 0
So 6971-74-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO3S/c1-11-7-9-13(10-8-11)19(17,18)15-14(16)12-5-3-2-4-6-12/h2-10H,1H3,(H,15,16)

6971-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylphenyl)sulfonylbenzamide

1.2 Other means of identification

Product number -
Other names F0898-0188

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:6971-74-0 SDS

6971-74-0Relevant articles and documents

Chemoselective Cleavage of Acylsulfonamides and Sulfonamides by Aluminum Halides

Sang, Dayong,Dong, Bingqian,Liu, Yunfeng,Tian, Juan

, p. 3586 - 3595 (2022/02/25)

The chemoselective cleavage of C-N bonds of amides, sulfonamides, and acylsulfonamides by aluminum halides is described. AlCl3and AlI3display complementary reactivities toward N-alkyl and N-acyl moieties. N-Alkylacylsulfonamides, sec

Ru(ii)-catalyzed allenylation and sequential annulation of: N -tosylbenzamides with propargyl alcohols

Kumar, Shreemoyee,Nair, Akshay M.,Volla, Chandra M. R.

, p. 6280 - 6283 (2021/07/02)

We hereby report Ru(ii)-catalyzed C(sp2)-H allenylation of N-tosylbenzamides to access multi-substituted allenylamides. Furthermore, the allenylamides were converted to the corresponding isoquinolone derivatives via base mediated annulation. The current protocol features low catalyst loading, mild reaction conditions, high functional group compatibility and desired scalability. The unique functionality of the afforded allenes allowed further transformations to expand the practicality of the protocol. This journal is

NOVEL AMIDATION METHOD

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Paragraph 0104-0110; 0121, (2021/09/21)

The present invention relates to a novel amidation process. To the present invention, an active N -center radical activated by light irradiation can be utilized to provide a selective amidation method. In addition, the present invention can provide an amide compound derived from an aldehyde having a functional group of various aspects, and is expected to be applicable to various technical fields.

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