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Phosphorane, chlorobis(1,1-dimethylethyl)(diphenylmethylene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81176-00-3

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81176-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81176-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,7 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81176-00:
(7*8)+(6*1)+(5*1)+(4*7)+(3*6)+(2*0)+(1*0)=113
113 % 10 = 3
So 81176-00-3 is a valid CAS Registry Number.

81176-00-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name benzhydrylidene-ditert-butyl-chloro-λ<sup>5</sup>-phosphane

1.2 Other means of identification

Product number -
Other names Phosphorane,chlorobis(1,1-dimethylethyl)(diphenylmethylene)

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:81176-00-3 SDS

81176-00-3Relevant academic research and scientific papers

REACTIONS OF STERICALLY HINDERED PHOSPHINES WITH CARBON TETRAHALIDES: P-HALOGENYLIDS

Kolodyazhnyi, O. I.

, p. 2125 - 2137 (2007/10/02)

1.A study has been made of the effects of steric factors on the reactions of tertiary phosphines with carbon tetrahalides.It is found that in the interaction of sterically hindered phosphine with carbon tetrabromide one gets the formation of bromophosphonium tribromomethylid, which exists at a low temperature, this being in an ionic pair containing the anion CBr3-.A sterically hindered phosphine having hydrogen at the α carbon atom forms P-halogenylids on reaction with carbon tetrahalides. 2.Unstabilized P-halogenylids with unsubstituted methylene and alkylidene gr oups have been synthesized, and also P-halogenylids with trimethylsilyl, methyl sulfide, phosphine, acyl, and aromatic groups on the ylid carbon atom. 3.A study has been made of the reactions of P-chlorylids with chlorine-bearing electrophilic reagents , which give rise to new P-halogenylids.

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