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1-Cyclohexyl-4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoro-undec-2-yn-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95541-00-7

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95541-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95541-00-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,5,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95541-00:
(7*9)+(6*5)+(5*5)+(4*4)+(3*1)+(2*0)+(1*0)=137
137 % 10 = 7
So 95541-00-7 is a valid CAS Registry Number.

95541-00-7Downstream Products

95541-00-7Relevant academic research and scientific papers

AN EFFICIENT SYNTHESIS OF α-F-ALKYNYLATED ALCOHOLS BY NEW SILOXANE-FLUORIDE ION CATALYZED REACTION OF 1H-F-1-ALKENEPHOSPHONATES WITH ALDEHYDES

Ishihara, Takashi,Maekawa, Takashige,Ando, Teiichi

, p. 357 - 360 (2007/10/02)

1H-F-1-Alkenephosphonates react smoothly with a variety of aldehydes under the influence of catalytic amounts of hexamethyldisiloxane and tetrabutylammonium fluoride at room temperature to afford the corresponding α-F-alkynylated alcohols in good to excel

NEW FLUORIDE ION-CATALYZED REACTION OF F-ALKYLACETYLENES WITH SILYL ENOL ETHERS. AN EFFICIENT ROUTE TO F-ALKYL-SUBSTITUTED PROPAPGYLIC ALCOHOLS AND α-HYDROXY KETONES

Ishihara, Takashi,Yamasaki, Yasuhiro,Ando, Teiichi

, p. 79 - 82 (2007/10/02)

Treatment of F-alkylacetylenes, generated in situ from 1H-F-1-alkenephosphonates, with silyl enol ethers in the presence of a catalytic amount of tetrabutylammonium fluoride gives good yields of F-alkyl-substituted propargyl alcohols or 4-(1H-F-alkylidene)-1,3-dioxolane derivatives, the latter being converted to the corresponding α-hydroxy ketones.

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