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1-Pentanone, 1-[1,1'-biphenyl]-4-yl-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59662-30-5

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59662-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59662-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,6 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59662-30:
(7*5)+(6*9)+(5*6)+(4*6)+(3*2)+(2*3)+(1*0)=155
155 % 10 = 5
So 59662-30-5 is a valid CAS Registry Number.

59662-30-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1-(4-phenylphenyl)pentan-1-one

1.2 Other means of identification

Product number -
Other names 1-Pentanone,1-[1,1'-biphenyl]-4-yl-4-methyl

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:59662-30-5 SDS

59662-30-5Downstream Products

59662-30-5Relevant academic research and scientific papers

Well-defined Ir/Pd complexes with a triazolyl-diylidene bridge as catalysts for multiple tandem reactions

Zanardi, Alessandro,Mata, Jose A.,Peris, Eduardo

, p. 14531 - 14537 (2009)

The ligand 1,2,4-trimethyl-triazolyl-diylidene has been used for the preparation of a series of three iridium/palladium heterometallic complexes that have been fully characterized. The presence of the two different metals allows tandem processes to be designed by combining reactions that are typically catalyzed by Ir and Pd. Three tandem reactions have been studied: dehalogenation/transfer hydrogenation of haloacetophenones, Suzuki-coupling/ transfer hydrogenation of p-bromoacetophenone, and Suzukicoupling/ α-alkylation of p-bromoacetophenone. All three reactions yielded excellent outcomes to the corresponding final products, with the relevant feature that the heterodimetallic complexes are more active than the sum of the corresponding homodimetallic species. All three catalytic reactions reported here constitute unprecedented examples of tandem approaches to complex organic molecules.

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