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Benzenamine, 2,4,6-tris(1,1-dimethylethyl)-N-(phenylphosphinidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109874-39-7

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109874-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109874-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,7 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 109874-39:
(8*1)+(7*0)+(6*9)+(5*8)+(4*7)+(3*4)+(2*3)+(1*9)=157
157 % 10 = 7
So 109874-39-7 is a valid CAS Registry Number.

109874-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-(2,4,6-tritert-butylphenyl)iminophosphane

1.2 Other means of identification

Product number -
Other names P-phenyl-N-(2,4,6-tri-tert-butylphenyl)phosphinimine

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:109874-39-7 SDS

109874-39-7Relevant academic research and scientific papers

Reactions of Halogen (2,4,6-tri-tert-butylphenylimino)phosphine Complexes with Electrophiles and Nucleophiles: Abstraction or Substitution of the Halogen

Niecke, E.,Nixon, J. F.,Wenderoth, P.,Passos, B. F. Trigo,Nieger, M.

, p. 846 - 848 (2007/10/02)

The structure of the first nickel halogeniminophosphine complex, i.e. (PEt3)2Ni(X-P=NAr)2 (Ar = 2,4,6-tri-tert-butylphenyl); X = Cl is reported; reactions of this and related compounds with AlCl3 afford the cationic complexes 7-10; the alkyliminophosphine complexes 12 and 13 are obtained by treatment of the chloroiminophosphine complexes 1a and 4a with Grignard reagent.

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