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Phosphine, tris([1,1':3',1''-terphenyl]-5'-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

561068-06-2

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561068-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 561068-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,1,0,6 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 561068-06:
(8*5)+(7*6)+(6*1)+(5*0)+(4*6)+(3*8)+(2*0)+(1*6)=142
142 % 10 = 2
So 561068-06-2 is a valid CAS Registry Number.

561068-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tris(3,5-diphenylphenyl)phosphane

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:561068-06-2 SDS

561068-06-2Downstream Products

561068-06-2Relevant academic research and scientific papers

Synthesis of a new, bulky tetraarylphosphonium, a tetraarylborate, and their salt

Matsumoto, Kaya,Hatano, Keiichiro,Umezawa, Naoki,Higuchi, Tsunehiko

, p. 2181 - 2185 (2007/10/03)

Tris(m-terphenyl-5′-yl)phosphine (2), tetrakis(m-terphenyl-5′- yl)phosphonium bromide (3), sodium tetrakis(m-terphenyl-5′-yl)borate (4), and the phosphonium borate salt 5 of 3 and 4 were synthesized, in the expectation of creating interionic spacings that

Rate enhancement with a bowl-shaped phosphane in the rhodium-catalyzed hydrosilylation of ketones

Niyomura, Osamu,Tokunaga, Makoto,Obora, Yasushi,Iwasawa, Tetsuo,Tsuji, Yasushi

, p. 1287 - 1289 (2007/10/03)

Up to 154-fold rate enhancement (see picture) and higher yields are achieved with the bowl-shaped triarylphosphane ligand P(tm-tp)3 compared with common phosphane ligands in Rh-catalyzed hydrosilylation of ketones. The superior performance of P(tm-tp)3 over the similar P(tp)3 is apparently related to the deeper bowl formed by the methyl-bearing terphenyl substituents in the former.

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