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Phosphine, [(chlorodimethylsilyl)methyl]diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72447-46-2

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72447-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72447-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,4,4 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72447-46:
(7*7)+(6*2)+(5*4)+(4*4)+(3*7)+(2*4)+(1*6)=132
132 % 10 = 2
So 72447-46-2 is a valid CAS Registry Number.

72447-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [chloro(dimethyl)silyl]methyl-diphenylphosphane

1.2 Other means of identification

Product number -
Other names chlorodimethylsilyl(diphenylphosphino)methane

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:72447-46-2 SDS

72447-46-2Relevant academic research and scientific papers

Ethylene oligomerization promoted by nickel-based catalysts with silicon-bridged diphosphine amine ligands

Wei, Wei,Yu, Buwei,Alam, Fakhre,Huang, Yongwang,Cheng, Shaoling,Jiang, Tao

, p. 125 - 133 (2018/10/02)

A series of nickel complexes [Ni(L1)Br2] (C1), [Ni(L2)Br2] (C2) and [Ni(L3)Br2] (C3) (L1 = N-isopropyl-N-(((diphenylphosphanyl)methyl)dimethylsilyl)-1,1-diphenylphosphanamine, L2 = N-cyclopentyl-N-(((diphenylphosphanyl)methyl)dimethylsilyl)-1,1-diphenylphosphanamine, L3 = N-(2,6-diisopropylphenyl)-N-(((diphenylphosphanyl)methyl)dimethylsilyl)-1,1-diphenylphosphanamine) were synthesized and characterized by elemental analysis, mass spectrometry, spectroscopy and single-crystal X-ray diffraction. L1, L2 and L3 each act as bidentate ligands. Upon activation with ethylaluminum dichloride, these complexes produce efficient catalytic systems for selective dimerization of ethylene to 1-butene, with catalytic activities of 3.45 × 107?g/(molNi·h) and 95.6% butene selectivity containing 87.6% 1-butene fraction.

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