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1H-Pyrazole, 1-[2-(diphenylphosphino)phenyl]-3,5-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

709045-72-7

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709045-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 709045-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,9,0,4 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 709045-72:
(8*7)+(7*0)+(6*9)+(5*0)+(4*4)+(3*5)+(2*7)+(1*2)=157
157 % 10 = 7
So 709045-72-7 is a valid CAS Registry Number.

709045-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-(3,5-dimethylpyrazol-1-yl)phenyl]-diphenylphosphane

1.2 Other means of identification

Product number -
Other names 1-(2-diphenylphoshanylphenyl)-3,5-dimethyl-1H-pyrazole

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:709045-72-7 SDS

709045-72-7Relevant academic research and scientific papers

Pyrazole-tethered arylphosphine ligands for Suzuki reactions of aryl chlorides: How important is chelation?

Mukherjee, Anuradha,Sarkar, Amitabha

, p. 9525 - 9528 (2007/10/03)

Pyrazole-derived bidentate ligands (P,N-donor) with bulky substituents at the 3-position of the pyrazole, 1b-d, were used with Pd2(dba) 3 to carry out efficient Suzuki coupling reactions with both aryl bromides and chlorides. Enhanced catalytic activity on account of steric crowding in the metal complex suggested participation of a chelated structure in the intermediate catalytic steps.

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