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Phosphonic acid, [difluoro(phenylseleno)methyl]-, diethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

327156-99-0

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327156-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 327156-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,7,1,5 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 327156-99:
(8*3)+(7*2)+(6*7)+(5*1)+(4*5)+(3*6)+(2*9)+(1*9)=150
150 % 10 = 0
So 327156-99-0 is a valid CAS Registry Number.

327156-99-0SDS

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 [diethoxyphosphoryl(difluoro)methyl]selanylbenzene

1.2 Other means of identification

Product number -
Other names diethyl phenylselanyldifluoromethylphosphonate

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:327156-99-0 SDS

327156-99-0Relevant academic research and scientific papers

Phosphonodifluoromethyl and phosphonothiodifluoromethyl radicals. Generation and addition onto alkenes and alkynes

Pignard, Sebastien,Lopin, Chrystel,Gouhier, Geraldine,Piettre, Serge R.

, p. 31 - 37 (2007/10/03)

Selanylated difluoromethylphosphonates and difluoromethylphosphonothioates are good precursors to phosphonodifluoromethyl and phosphonothiodifluoromethyl radicals, respectively. When generated in the presence of alkenes and a hydrogen donor, the corresponding α,α-difluorinated alkylphosphonates or alkylphosphonothioates are produced in fair to good yields. The use of alkynes results in the formation of α,α-difluorinated allyl derivatives in useful yields. The presence of the sulfur atom in phosphonothiodifluoromethyl radicals usually translates into higher isolated yields.

Sulfanyl- and selanyldifluoromethylphosphonates as a source of phosphonodifluoromethyl radicals and their addition onto alkenes

Lequeux, Thierry,Lebouc, Fanny,Lopin, Chrystel,Yang, Hongli,Gouhier, Geraldine,Piettre, Serge R.

, p. 185 - 188 (2007/10/03)

equation presented Two different strategies are shown to produce sulfanyl and selanyldifluoromethylphosphonates. Thus, treatment of sulfanyldichloromethylphosphonates by 3HF-NEt3 in the presence of zinc bromide produces the corresponding sulfan

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