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Benzonitrile, 4-[2-(diphenylphosphinothioyl)ethenyl]-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82943-04-2

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82943-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82943-04-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,4 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82943-04:
(7*8)+(6*2)+(5*9)+(4*4)+(3*3)+(2*0)+(1*4)=142
142 % 10 = 2
So 82943-04-2 is a valid CAS Registry Number.

82943-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-4-(2-(diphenylphosphorothioyl)vinyl)benzonitrile

1.2 Other means of identification

Product number -
Other names -

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:82943-04-2 SDS

82943-04-2Downstream Products

82943-04-2Relevant academic research and scientific papers

Synthesis of α,β-Unsaturated Phosphine Sulfides

Chen, Jin-Xiang,Jia, Xue-Shun,Wang, Xian-Liang,Yin, Liang

, p. 141 - 149 (2019/12/26)

α,β-Unsaturated phosphine sulfides may exhibit different reactivity from α,β-unsaturated phosphine oxides toward nucleophilic addition and thus may find new applications in copper(I)-catalyzed asymmetric reactions. Herein, various α,β-unsaturated phosphine sulfides were prepared in moderate to excellent yields from the parent α,β-unsaturated phosphine oxides with Lawesson's reagent. The reaction enjoys a broad substrate scope and tolerates a variety of functional groups.

Preparation of β-Substituted trans-Ethylene Diphenylphosphines and Sulphides by P(O) and P(S)-activated Olefination

Gloyna, Dieter

, p. 360 - 366 (2007/10/02)

Methylene bis-diphenylphosphine monoxide (3c) in toluene reacts regiospecifically and stereoselectively with aldehydes in the presence of potassium tert-butoxide to β-substituted trans-ethylene diphenylphosphines 6, which can be oxidized to the sulphides 2 by sulphur in acetone.These sulphides 2 are to be obtained also directly from methylene bis-diphenylphosphine oxide sulphide 3b and methylene bis-diphenylphosphine disulphide 3d, respectively, under the same olefination conditions.But the yields are smaller and the purification of the raw products is much more difficult, if 3d is used.

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