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Phosphine, phenylbis[2-(2-phenylethenyl)phenyl]-, (E,E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81631-34-7

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81631-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81631-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,3 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81631-34:
(7*8)+(6*1)+(5*6)+(4*3)+(3*1)+(2*3)+(1*4)=117
117 % 10 = 7
So 81631-34-7 is a valid CAS Registry Number.

81631-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Phenyl-bis[2-(trans-2-phenylethenyl)phenyl]phosphan

1.2 Other means of identification

Product number -
Other names Phenylbis[2-(trans-2-phenylethenyl)phenyl]phosphan

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:81631-34-7 SDS

81631-34-7Downstream Products

81631-34-7Relevant academic research and scientific papers

Synthesis of Triphenylphosphane-en-ynes and Phosphindoles as well as X-Ray Analyses of two Phosphindoles

Butters, Thomas,Winter, Werner

, p. 990 - 1002 (2007/10/02)

By means of aminochlorophenylphosphanes triphenylphosphanes are prepared, in which the o-positions are optionally substituted by trans-phenylethenyl and phenylethinyl groups (4a - c and 5a - c).Surprisingly, the intermediate chlorophosphanes 3a and c can

Addition of Water to o-Phenylethinyl-substituted Triphenylphosphanes and Reduction of the Formed Phosphane Oxide En-ynes

Butters, Thomas,Haller-Pauls, Irene,Winter, Werner

, p. 578 - 592 (2007/10/02)

Heating of the o-phenylethinyl-substituted triphenylphosphanes 1a - c in organic solvents containing water affords the phosphane oxides 2a - c through an intramolecular nucleophilic addition of the phosphorus to the triple bond, stereoselectively with a t

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