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89358-50-9

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89358-50-9 Usage

Type of compound

Ketone

Structure

Diphenylphosphinyl group attached to the third carbon of the butanone chain
Phenyl group attached to the first carbon

Usage

Organic synthesis as a reagent or catalyst
Formation of carbon-carbon bonds
Reduction of organic compounds

Potential applications

Pharmaceutical industry
Agricultural industry

Unique properties

Facilitates various chemical reactions
Offers versatility in synthetic chemistry
These properties and specific content provide a comprehensive overview of 1-Butanone, 3-(diphenylphosphinyl)-1-phenyl(DPPE ketone), highlighting its structure, applications, and unique characteristics in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 89358-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,5 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89358-50:
(7*8)+(6*9)+(5*3)+(4*5)+(3*8)+(2*5)+(1*0)=179
179 % 10 = 9
So 89358-50-9 is a valid CAS Registry Number.

89358-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-diphenylphosphoryl-1-phenylbutan-1-one

1.2 Other means of identification

Product number -
Other names 3-diphenylphosphinoyl-1-phenylbutan-1-one

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:89358-50-9 SDS

89358-50-9Relevant articles and documents

Palladium(II)-catalyzed conjugate phosphination of electron-deficient acceptors

Trepohl, Verena T.,Mori, Susumu,Itami, Kenichiro,Oestreich, Martin

supporting information; experimental part, p. 1091 - 1094 (2009/07/25)

A general protocol for the conjugate transfer of diphenyl-, dicyclohexyl-, and di-tert-butylphosphinyl groups from silylphosphines to cyclic and acyclic electron-deficient acceptors employing a bench-stable palladium(II) catalyst is reported. Several Eand

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