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(S)-1,1,1-trifluoro-4-(5-fluoro-2-methylphenyl)-4-methyl-2-((R)-toluene-4-sulfinylmethyl)pentan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

866943-85-3

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866943-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 866943-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,9,4 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 866943-85:
(8*8)+(7*6)+(6*6)+(5*9)+(4*4)+(3*3)+(2*8)+(1*5)=233
233 % 10 = 3
So 866943-85-3 is a valid CAS Registry Number.

866943-85-3Relevant academic research and scientific papers

GLUCOCORTICOID MIMETICS, METHODS OF MAKING THEM, PHARMACEUTICAL COMPOSITIONS, AND USES THEREOF

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Page/Page column 66, (2009/12/28)

Compounds of Formula I wherein R1, R2, X, and Y are as defined herein, or a tautomer, optical isomer, prodrug, co-crystal, or salt thereof; pharmaceutical compositions containing such compounds, and methods of modulating the glucocorticoid receptor function and methods of treating disease-states or conditions mediated by the glucocorticoid receptor function or characterized by inflammatory, allergic, or proliferative processes in a patient using these compounds.

A concise asymmetric route for the synthesis of a novel class of glucocorticoid mimetics containing a trifluoromethyl-substituted alcohol

Lee, Thomas W.,Proudfoot, John R.,Thomson, David S.

, p. 654 - 657 (2007/10/03)

An asymmetric route was developed for the synthesis of a class of novel glucocorticoid receptor ligand derivatives 1. The key step of this synthesis involves a diastereoselective addition of chiral sulfoxide anion to a trifluoromethyl ketone precursor. Th

Stereoselective synthesis of certain trifluoromethyl-substituted alcohols

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Page/Page column 8, (2010/02/14)

A process for stereoselective synthesis of a compound of Formula (X) or Formula (X′) wherein R1, R2, and R3 are as defined herein, the process comprising: (a) reacting the starting material of formula A with a chiral sulfo

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