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Benzenepropanethioamide, N,N-dimethyl-a-2-propenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88431-07-6

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88431-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88431-07-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,3 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88431-07:
(7*8)+(6*8)+(5*4)+(4*3)+(3*1)+(2*0)+(1*7)=146
146 % 10 = 6
So 88431-07-6 is a valid CAS Registry Number.

88431-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-2-benzylthiopent-4-enamide

1.2 Other means of identification

Product number -
Other names 2-Benzyl-pent-4-enethioic acid dimethylamide

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:88431-07-6 SDS

88431-07-6Downstream Products

88431-07-6Relevant academic research and scientific papers

Pd-catalyzed allylic alkylation of thioamides

Rong, Bin,Ding, Lei,Yu, Hailei,Yang, Qin,Liu, Xuliang,Xu, Dongfang,Li, Guisheng,Zhao, Baoguo

, p. 6501 - 6503 (2013)

This work describes the first Pd-catalyzed allylic alkylation of thioamides. Various thioamides were efficiently α-allylated in high yields and with excellent selectivity for monoallylation under mild reaction conditions. The process not only provides a facile method for the synthesis of functionalized thioamides, but also presents a useful transformation for synthetically important thioamides.

1,3-Asymmetric Induction: Highly Stereoselective Synthesis of 2,4-Trans-Disubstituted γ-Butyrolactones and γ-Butyrothiolactones

Tamaru, Yoshinao,Mizutani, Masato,Furukawa, Yutaka,Kawamura, Shin-ichi,Yoshida, Zen-ichi,et al.

, p. 1079 - 1085 (2007/10/02)

A novel 1,3-trans asymmetric induction has been observed for the halolactonization of α- and α,β-substituted γ,δ-unsaturated amides.The 1,3-trans selectivity is lost in the threo diastereomers of amides with β-OH or β-OAc substituent, due to the 1,2-cis d

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