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Arsine, bis(2-methylphenyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58194-61-9

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58194-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58194-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,9 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58194-61:
(7*5)+(6*8)+(5*1)+(4*9)+(3*4)+(2*6)+(1*1)=149
149 % 10 = 9
So 58194-61-9 is a valid CAS Registry Number.

58194-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(2-methylphenyl)-phenylarsane

1.2 Other means of identification

Product number -
Other names -

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:58194-61-9 SDS

58194-61-9Downstream Products

58194-61-9Relevant academic research and scientific papers

A practical screening strategy of arsenic ligands for a transition-metal-catalyzed reaction

Imoto, Hiroaki,Yamazawa, Chieko,Tanaka, Susumu,Kato, Takuji,Naka, Kensuke

, p. 821 - 823 (2017)

Organoarsenic ligands were synthesized via a safe and easy procedure, superior to the conventional synthetic methodologies. Diiodophenylarsine was prepared in situ, and was readily converted to diarylphenylarsines. Pd-catalyzed Mizoroki-Heck reaction was investigated using the obtained arsenic ligands. It was found that bulky and electron-donating ligands were effective for the reaction, meaning that the success in the screening of arsenic ligand structures was based on the present facile strategy.

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