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Phosphine sulfide, (3,7-dimethyl-2,6-octadienyl)diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

828282-67-3

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828282-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828282-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,2,8 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 828282-67:
(8*8)+(7*2)+(6*8)+(5*2)+(4*8)+(3*2)+(2*6)+(1*7)=193
193 % 10 = 3
So 828282-67-3 is a valid CAS Registry Number.

828282-67-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-dimethylocta-2,6-dienyl-diphenyl-sulfanylidene-λ<sup>5</sup>-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:828282-67-3 SDS

828282-67-3Downstream Products

828282-67-3Relevant academic research and scientific papers

nBuLi-mediated hydrophosphination: A simple route to valuable organophosphorus compounds

Perrier, Arnaud,Comte, Virginie,Moise, Claude,Richard, Philippe,Le Gendre, Pierre

experimental part, p. 1562 - 1568 (2010/06/15)

A straightforward synthesis of homoallyl- and allylphosphanes has been developed using nBuLi-mediated hydrophosphination of conjugated dienes. In all the cases the phosphorus atom of the reacting phosphane attacked the sterically less demanding side of the diene exclusively. In addition, high regioselectivities towards 1,2- or 1,4-addition products were observed depending on the nature of the dienes. This hydrophosphination reaction was extended to a variety of substrates such as styrene derivatives, alkynes and 1,3,5-cycloheptatriene. The structures of three hydrophosphination products were confirmed by X-ray diffraction studies.

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