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86823-71-4

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86823-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86823-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,8,2 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 86823-71:
(7*8)+(6*6)+(5*8)+(4*2)+(3*3)+(2*7)+(1*1)=164
164 % 10 = 4
So 86823-71-4 is a valid CAS Registry Number.

86823-71-4SDS

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 (Z)-1-(phenylsulfonyl)oct-2-ene

1.2 Other means of identification

Product number -
Other names [((Z)-Oct-2-ene)-1-sulfonyl]-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:86823-71-4 SDS

86823-71-4Downstream Products

86823-71-4Relevant articles and documents

Reciprocal-Activation Strategy for Allylic Sulfination with Unactivated Allylic Alcohols

Xie, Peizhong,Sun, Zuolian,Li, Shuangshuang,Cai, Xinying,Qiu, Ju,Fu, Weishan,Gao, Cuiqing,Wu, Shisheng,Yang, Xiaobo,Loh, Teck-Peng,Loh, Teck-Peng

supporting information, p. 4893 - 4897 (2020/06/24)

A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was developed. In this reaction, the hydrogen bond interaction between allylic alcohols and sulfinic acids allowed for reciprocal activation, which enabled a dehydrative cross-coupling process to occur under mild reaction conditions. This reaction worked in an environmentally friendly manner, yielding water as the only byproduct. A variety of allylic sulfones could be obtained in good to excellent yields with wide functional group tolerance. In gram scale reactions, allylic sulfones could be conveniently isolated in high yield by filtration.

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