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Phosphine oxide, [(1E)-1-methoxy-3-methyl-1-propene-1,3-diyl]bis[diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87953-00-2

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87953-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87953-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,5 and 3 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87953-00:
(7*8)+(6*7)+(5*9)+(4*5)+(3*3)+(2*0)+(1*0)=172
172 % 10 = 2
So 87953-00-2 is a valid CAS Registry Number.

87953-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1,3-Bis(diphenylphosphoryl)-1-butenyl)-methyl-ether

1.2 Other means of identification

Product number -
Other names [1,3-Bis(diphenylphosphoryl)-1-butenyl]-methyl-ether

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:87953-00-2 SDS

87953-00-2Relevant academic research and scientific papers

THE REACTIONS OF α-ALKOXYALLYLPHOSPHINE OXIDE YLIDES WITH SILICON, SULPHUR AND PHOSPHORUS ELECTROPHILES

Devchand, Dipak K.,Murray, Alistair W.,Smeaton, Elizabeth

, p. 4635 - 4638 (2007/10/02)

Anions (2), derived from α-methoxyallylphosphine oxides (1), react with silicon, sulphur and phosphorus electrophiles in a highly regioselective fashion to give the products of γ-attack.

The Reactive Behaviour of Methyl Substituted Propenoyldiphenylphosphanes and their Oxides

Lindner, Ekkehard,Tamoutsidis, Efstathios

, p. 3141 - 3150 (2007/10/02)

The action of RC(O)Cl (1a - e) on (CH3)3SiPPh2 generates only the propenoyldiphenylphosphanes RC(O)PPh2 2c - e, in the case of 2a, b polymerization and decomposition, respectivel

Synthesis, Structure, and Isomerism of Stable Diphosphorylated Enols

Lindner, Ekkehard,Tamoutsidis, Efstathios,Hiller, Wolfgang,Fawzi, Riad

, p. 3151 - 3163 (2007/10/02)

Under addition of the intermediary formed HP(O)Ph2 to the double bond of 1a - c the hydrolysis of the unsaturated acyldiphenylphosphane oxides R1R2C=CR3C(O)P(O)Ph2 (1a - c) yields the E-isomeric phosphorylated enols Ph2(O)

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