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2,2-difluoro-1-phenyl-dec-3-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

916332-83-7

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916332-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 916332-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,3,3 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 916332-83:
(8*9)+(7*1)+(6*6)+(5*3)+(4*3)+(3*2)+(2*8)+(1*3)=167
167 % 10 = 7
So 916332-83-7 is a valid CAS Registry Number.

916332-83-7Relevant academic research and scientific papers

Lanthanide triflate-catalyzed preparation of β,β- difluorohomopropargyl alcohols in aqueous media. Application to the synthesis of 4,4-difluoroisochromans

Arimitsu, Satoru,Hammond, Gerald B.

, p. 8665 - 8668 (2006)

An indium-mediated Barbier-type reaction of difluoropropargyl bromide with several aldehydes in aqueous media was enhanced by a catalytic amount of a lanthanide triflate (5 mol %). The reaction gave the corresponding β,β-difluorohomopropargyl alcohols wit

Supported gold nanoparticles catalyzed: Cis -selective semihydrogenation of alkynes using ammonium formate as the reductant

Liang, Shengzong,Hammond, Gerald B.,Xu, Bo

, p. 6013 - 6016 (2016/05/24)

TiO2 supported gold nanoparticles with low loading (0.5 mol%) are able to semihydrogenate non-fluorinated and gem-difluorinated alkynes to cis-alkenes with high selectivity, using cost-effective and easy-to-handle ammonium formate as the reductant. No over-reduction was observed. The good recyclability of Au/TiO2 allows for "green" semireduction of alkynes. A difluorinated pyran and α,β-unsaturated δ-lactone were easily prepared from the obtained gem-difluoro alkene building blocks.

gem-Difluoropropargylation of aldehydes using cat. In/Zn in aqueous media

Arimitsu, Satoru,Jacobsen, Jesse M.,Hammond, Gerald B.

, p. 1625 - 1627 (2008/02/03)

Zn (0.9 equiv) in combination with catalytic amounts of In (0.1 equiv) and I2 (0.1 equiv) was found to effect the reaction of several difluoropropargyl bromide derivatives with aldehydes to produce gem-difluorohomopropargyl alcohols in aqueous

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