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18462-38-9

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18462-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18462-38-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,6 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18462-38:
(7*1)+(6*8)+(5*4)+(4*6)+(3*2)+(2*3)+(1*8)=119
119 % 10 = 9
So 18462-38-9 is a valid CAS Registry Number.

18462-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-nitro-4-(2-(phenylsulfonyl)vinyl)benzene

1.2 Other means of identification

Product number -
Other names 1-((E)-2-Benzenesulfonyl-vinyl)-4-nitro-benzene

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:18462-38-9 SDS

18462-38-9Downstream Products

18462-38-9Relevant articles and documents

Vinyl sulfone synthesisviacopper-catalyzed three-component decarboxylative addition

An, Seunghwan,Lee, Sunwoo,Song, Kwang Ho

supporting information, p. 7827 - 7831 (2021/09/28)

The synthesis of vinyl sulfone derivativesviathe reaction of arylpropiolic acids, K2S2O5, and aryl boronic acids is reported. The CuBr2/1,10-phenanthroline catalytic system in the presence of acetic acid provide

Synthesis of Vinyl Sulfones via I2-mediated Alkene Sulfonylations with Thiosulfonates

Hwang, Sang Joon,Shyam, Pranab K.,Jang, Hye-Young

supporting information, p. 535 - 539 (2018/03/13)

A simple sulfonylation strategy involving I2 and thiosulfonates, as sulfonyl-group precursors, is reported for the synthesis of vinyl sulfones. Sulfonyl radicals are presumed to be generated from thiosulfonates, which subsequently react with st

Electrosynthesis of (E)-Vinyl Sulfones Directly from Cinnamic Acids and Sodium Sulfinates via Decarboxylative Sulfono Functionalization

Qian, Peng,Bi, Meixiang,Su, Jihu,Zha, Zhenggen,Wang, Zhiyong

, p. 4876 - 4882 (2016/07/06)

A variety of (E)-vinyl sulfones were constructed directly from cinnamic acids and sodium sulfinates with high regioselectivity at room temperature by virtue of an electrocatalytic oxidation. A radical intermediate was detected, and the corresponding mecha

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