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3-(Hydroxymethyl)sulphur pentafluoride, 3-(Pentafluorosulphanyl)benzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

773872-71-2

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773872-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773872-71-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,8,7 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 773872-71:
(8*7)+(7*7)+(6*3)+(5*8)+(4*7)+(3*2)+(2*7)+(1*1)=212
212 % 10 = 2
So 773872-71-2 is a valid CAS Registry Number.

773872-71-2Downstream Products

773872-71-2Relevant academic research and scientific papers

Racemic and enantioselective metal-catalyzed synthesis of SF5-containing diarylmethanols

Desroches, Justine,Tremblay, Ariane,Paquin, Jean-Fran?ois

, p. 8764 - 8780 (2016/10/03)

The racemic and enantioselective metal-catalyzed addition of arylboronic acids to 4- and 3-(pentafluorosulfur)benzaldehydes is reported. The racemic synthesis was accomplished using a Pd-based system and a wide range of arylboronic acids could be used, resulting in yields of 42 to 98% of the corresponding SF5-containing diarylmethanols. A ruthenium-based system, along with (R,R)-Me-BIPAM as the chiral ligand, was investigated and optimized for the enantioselective version. In this case, while the chiral SF5-containing diarylmethanols were generally obtained in good yields (up to 94%) and enantioselectivities (up to 98% ee), limitations were also observed. For instance, 4-(pentafluorosulfur)benzaldehyde generally provided slightly better yields than 3-(pentafluorosulfur)benzaldehyde. In addition, lower yields and enantioselectivities were observed when using either 4- and 3-substituted arylboronic acids bearing electron-withdrawing (e.g., CO2Et, NO2, CF3) or 2-substituted arylboronic acids (regardless of the nature of the substituent). Overall, the SF5-containing diarylmethanols described herein represent novel and potentially useful fluorinated building blocks for the synthesis of biologically active compounds.

Novel phenyl-substituted imidazolidines, process for preparation thereof, medicaments comprising said compounds and use thereof

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Page/Page column 41, (2011/08/04)

The invention relates to compounds of formula (I) wherein the groups have stated meanings, and to their physiologically compatible salts. Said compounds are suitable, for example, as anti-obesity drugs and for treating cardiometabolic syndrome.

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