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Methylisopropylphenylphosphine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36050-92-7

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36050-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36050-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,5 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 36050-92:
(7*3)+(6*6)+(5*0)+(4*5)+(3*0)+(2*9)+(1*2)=97
97 % 10 = 7
So 36050-92-7 is a valid CAS Registry Number.

36050-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl-phenyl-propan-2-ylphosphane

1.2 Other means of identification

Product number -
Other names Methylisopropylphenylphosphine

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:36050-92-7 SDS

36050-92-7Relevant academic research and scientific papers

A simple resolution procedure using the Staudinger reaction for the preparation of P-stereogenic phosphine oxides

Andersen,Ramsden,Che,Parvez,Keay

, p. 7478 - 7486 (2007/10/03)

The resolution of a variety of (±)-P-stereogenic phosphines is achieved by exploiting the Staudinger reaction of a (±)-phosphine with enantiopure (1S,2R)-O-(tert-butyldimethylsilyl)isobornyl-10-sulfonyl azide. The resulting mixtures of diastereomeric phosphinimines are generally separable by fractional crystallization or flash chromatography. Subsequent acid-catalyzed hydrolysis provides the corresponding optically pure phosphine oxides in high yields.

A novel synthesis of unsymmetrical tertiary phosphines: Selective nucleophilic substitution on phosphorus(III)

Singh, Sumita,Nicholas, Kenneth M.

, p. 149 - 150 (2007/10/03)

A new synthesis of unsymmetrical tertiary phosphines has been developed employing selective, sequential alkylation of chloroaminophospnines by Grignard and organolithium reagents.

Preparation of Alkylmethylphenylphosphines by the Method of Hewertson and Watson

Wolfsberger, Werner

, p. 295 - 298 (2007/10/02)

The reaction of C6H5(CH3)PNa with some alkyl halides in liquid ammonia was studied.The resulting phosphines were characterized by elemental analyses, NMR spectra, and by the reaction with trimethylsilyl azide giving trimethylsilylimino triorganophosphoranes. - Keywords: Alkylmethylphenylphosphines, N-Trimethylsilylimino Triorganophosphoranes, NMR Spectra

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