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923023-81-8

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923023-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923023-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,2 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 923023-81:
(8*9)+(7*2)+(6*3)+(5*0)+(4*2)+(3*3)+(2*8)+(1*1)=138
138 % 10 = 8
So 923023-81-8 is a valid CAS Registry Number.

923023-81-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-phenylethyl)phosphine selenide

1.2 Other means of identification

Product number -
Other names bis[2-(phenyl)ethyl]phosphine selenide

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:923023-81-8 SDS

923023-81-8Relevant articles and documents

Synthesis and structure of bis(2-phenylethyl) phosphine selenide

Sukhov,Gusarova,Ivanova,Bogdanova,Kazheva,Aleksandrov,D'Yachenko,Sinegovskaya,Malysheva,Trofimov

, p. 1066 - 1071 (2005)

Bis(2-phenylethyl)phosphine selenide was obtained with 86% yield from bis(2-phenylethyl)phosphine and selenium. XRD, IR, UV, and multinuclear NMR spectroscopic studies revealed that the phosphorus atom in the bis(2-phenylethyl)phosphine selenide molecule

Green synthesis of tertiary alkylselanylphosphine chalcogenides via catalyst-and solvent-free addition of secondary phosphine chalcogenides to vinyl selenides

Gusarova,Chernysheva,Yas'Ko,Trofimov

, p. 526 - 534 (2015/10/19)

Secondary phosphine sulfides and phosphine selenides react with vinyl selenides under mild conditions (80-82°C, without catalyst and solvent) to form regioselectively functionalized anti-Markovnikov adducts in high yield.

Reaction of vinyl selenides with secondary phosphines and elemental selenium: One-pot selective synthesis of a new family of diselenophosphinic se-esters

Artem'Ev, Alexander V.,Chernysheva, Nataliya A.,Gusarova, Nina K.,Yas'Ko, Svetlana V.,Liao, Jian-Hong,Liu,Albanov, Alexander I.,Trofimov, Boris A.

, p. 135 - 139 (2014/06/09)

Alkyl vinyl selenides react with diverse secondary phosphines and elemental selenium in a 1.1:1:2 molar ratio (120-124°C, 20-40 min, 1,4-dioxane) to afford selectively earlier unknown diselenophosphinic Se-esters, R 2P(Se)SeCH(Me)SeR, in 82-99%

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