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27831-94-3

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27831-94-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27831-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,3 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27831-94:
(7*2)+(6*7)+(5*8)+(4*3)+(3*1)+(2*9)+(1*4)=133
133 % 10 = 3
So 27831-94-3 is a valid CAS Registry Number.

27831-94-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitrophenyl)sulfonylbenzamide

1.2 Other means of identification

Product number -
Other names <4-Chlor-phenyl>-benzoyl-diimid

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:27831-94-3 SDS

27831-94-3Downstream Products

27831-94-3Relevant articles and documents

Pd-Catalyzed Asymmetric Synthesis of 3,4-Dihydroisoquinolinones From N-Ts-Benzamides and 1,3-Dienes

Kim, Tae Kyun,Youn, So Won

supporting information, p. 521 - 524 (2021/02/12)

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Vinylogous Elimination/C-H Functionalization/Allylation Cascade Reaction of Allenoate Adducts: Synthesis of Ring-Fused Dihydropyridinones

Sun, Manman,Chen, Weida,Wu, Haijian,Xia, Xiangyu,Yang, Jianguo,Wang, Lei,Shen, Guodong,Wang, Zhiming

, p. 8313 - 8319 (2020/11/03)

A palladium-catalyzed cascade reaction of β′-allenoate adducts with aryl/heteroaryl carboxamides through a vinylogous elimination/C-H functionalization/intramolecular allylation reaction sequence has been developed with high Z stereoselectivity. Various ring-fused dihydropyridinones bearing an α,β-unsaturated ester substituent are obtained. It is the first example of application of the allenoate adducts to C-H functionalization annulations as practical precursors of hard-to-get functionalized electron-deficient 1,3-butadienes. Using air as the terminal oxidant also shows a great advantage in environmental friendliness.

Palladium-Catalyzed C-H Trifluoroethoxylation of N-Sulfonylbenzamides

Yang, Long,Li, Shangda,Cai, Lei,Ding, Yongzheng,Fu, Lei,Cai, Zhihua,Ji, Huafang,Li, Gang

supporting information, p. 2746 - 2749 (2017/05/24)

The trifluoroethyl aryl ethers are important motifs in drug molecules. However, a report devoted specifically to the study of transition-metal-catalyzed C-H trifluoroethoxylation has not been reported to date. A protocol of Pd(II)-catalyzed o-C-H trifluor

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