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

61324-11-6

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61324-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61324-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,2 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61324-11:
(7*6)+(6*1)+(5*3)+(4*2)+(3*4)+(2*1)+(1*1)=86
86 % 10 = 6
So 61324-11-6 is a valid CAS Registry Number.

61324-11-6SDS

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 bis(3,5-dimethylpyrazol-1-yl)-phenylphosphane

1.2 Other means of identification

Product number -
Other names 3,5,3',5'-tetramethyl-1H,1'H-1,1'-phenylphosphanediyl-bis-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:61324-11-6 SDS

61324-11-6Relevant academic research and scientific papers

Nickel complexes incorporating pyrazole-based ligands for ethylene dimerization to 1-butylene

Wang, Tao,Dong, Bo,Chen, Yan-Hui,Mao, Guo-Liang,Jiang, Tao

, p. 388 - 392 (2015)

In this study we synthesized and characterized bis(3,5-dimethylpyrazolyl)dimethylsilane (L1) and bis(3,5-dimethylpyrazolyl)phenylphosphine (L2) and then prepared bidentate (NN) nickel complexes by reacting L1 or L2 with NiBr2(DME). In combination with methylaluminoxane, diethylchloroaluminum or ethyldichloroaluminum (EADC) as co-catalyst, L1/Ni and L2/Ni complexes exhibited moderate catalytic activities (240-1310 kg/molNi h) and high selectivities (up to 93.2%) for ethylene dimerization toward 1-butylene. The catalytic performance was substantially affected by the co-catalyst type and ligand environment, especially the bridge atom.

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