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Arsine, tris(4-fluorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

31734-75-5

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31734-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31734-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,3 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 31734-75:
(7*3)+(6*1)+(5*7)+(4*3)+(3*4)+(2*7)+(1*5)=105
105 % 10 = 5
So 31734-75-5 is a valid CAS Registry Number.

31734-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(4-fluorophenyl)arsane

1.2 Other means of identification

Product number -
Other names Tris-4-Fluorophenylarsin

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:31734-75-5 SDS

31734-75-5Upstream product

31734-75-5Downstream Products

31734-75-5Relevant academic research and scientific papers

Tertiary arsine ligands for the Stille coupling reaction

Chishiro, Akane,Imoto, Hiroaki,Inaba, Ryoto,Konishi, Masafumi,Naka, Kensuke,Yumura, Takashi

, p. 95 - 103 (2021/12/27)

The Stille coupling reaction is one of the most important coupling reactions. It is well known that the triphenylarsine ligand can accelerate the reaction rate of Stille coupling. However, other arsine ligands have never been investigated for the Stille c

An improved bidentate complex of iridium as a catalyst for hydrogen isotope exchange

Herbert, John M.,Kohler, Andrew D.,McNeill, Alan H.

, p. 285 - 294 (2007/10/03)

Iridium(I) complexes 1, containing bidentate phosphines, and 3, with arsine ligands, are generated in situ. These species mediate hydrogen isotope exchange in a variety of aromatic substrates including benzyl ketones. Although the catalytic activities of complexes 1 and 3 are generally unexceptional, a logical step leads to the use of [ethylene-1,2-bis(diphenylarsine)](cyclooctadiene) iridium(I) tetrafluoroborate (5), which is an efficient catalyst for both aryl and benzyl ketones, and mediates exchange to a substantial extent in other substrates also. Copyright

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