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(E)-3-phenyl-2-((phenylsulfonyl)methyl)acrylonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1126630-76-9

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1126630-76-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1126630-76-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,2,6,6,3 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1126630-76:
(9*1)+(8*1)+(7*2)+(6*6)+(5*6)+(4*3)+(3*0)+(2*7)+(1*6)=129
129 % 10 = 9
So 1126630-76-9 is a valid CAS Registry Number.

1126630-76-9Downstream Products

1126630-76-9Relevant academic research and scientific papers

A facile and mild synthesis of trisubstituted allylic sulfones from Morita-Baylis-Hillman carbonates

Jiang, Lin,Li, Yong-Gen,Zhou, Jiang-Feng,Chuan, Yong-Ming,Li, Hong-Li,Yuan, Ming-Long

, p. 8213 - 8222 (2015/05/20)

An efficient and catalyst-free synthesis of trisubstituted allylic sulfones through an allylic sulfonylation reaction of Morita-Baylis-Hillman (MBH) carbonates with sodium sulfinates has been developed. Under the optimized reaction conditions, a series of

Tetrabutylammonium iodide catalyzed allylic sulfonylation of Baylis-Hillman acetates with sulfonylhydrazides in water

Li, Xiaoqing,Xu, Xiangsheng,Tang, Yucai

, p. 1739 - 1742 (2013/04/10)

A tetrabutylammonium iodide catalyzed method for the synthesis of allyl aryl sulfone derivatives with Baylis-Hillman acetates and sulfonylhydrazides using tert-butyl hydroperoxide as an oxidation agent in water has been developed. In this process, the group eliminated from the sulfonyl precursor is molecular nitrogen.

An unexpected reaction of arenesulfonyl cyanides with allylic alcohols: Preparation of trisubstituted allyl sulfones

Reddy, Leleti Rajender,Hu, Bin,Prashad, Mahavir,Prasad, Kapa

experimental part, p. 172 - 174 (2009/04/10)

(Chemical Equation Presented) An efficient and practical protocol for the highly selective preparation of substituted allyl sulfones has been developed. Arenesulfonyl cyanides, Baylis-Hillman adducts, and simple allylic alcohols give an unforeseen outcome

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