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(S)-3-((2S,3R)-2-amino-3-(3,5-difluorophenyl)-4,4,4-trifluorobutanoyl)-4-benzyloxazolidin-2-one hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1104077-77-1

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1104077-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1104077-77-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,0,7 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1104077-77:
(9*1)+(8*1)+(7*0)+(6*4)+(5*0)+(4*7)+(3*7)+(2*7)+(1*7)=111
111 % 10 = 1
So 1104077-77-1 is a valid CAS Registry Number.

1104077-77-1Relevant academic research and scientific papers

Practical enantioselective synthesis of a 3-aryl-3-trifluoromethyl-2- aminopropanol derivative

Alimardanov, Asaf,Nikitenko, Antonia,Connolly, Terrence J.,Feigelson, Gregg,Chan, Anita W.,Ding, Zhixian,Ghosh, Mousumi,Shi, Xinxu,Ren, Jianxin,Hansen, Eric,Farr, Roger,MacEwan, Michael,Tadayon, Sam,Springer, Dane M.,Kreft, Anthony F.,Ho, Douglas M.,Potoski, John R.

experimental part, p. 1161 - 1168 (2010/04/22)

Development of a large-scale enantioselective synthesis of a lead compound containing a 3-aryl-3-trifluoromethyl-2-aminopropanol core is described. A single isomer of 3,3-disubstituted acrylic acid derivative was prepared via Perkin condensation or Horner

PROCESS FOR THE PREPARATION OF TRIFLUOROALKYL-PHENYL AND HETEROCYCLIC SULFONAMIDES

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Page/Page column 14, (2009/02/11)

A novel trifluoroacetylating agent, i.e., N-trifluoroacetylmorpholine, is described. This reagent is useful in the preparation of phenyl and heterocyclic sulfonamide compounds. Methods are therefore described for preparing sulfonamide compounds of the fol

PROCESSES AND INTERMEDIATES FOR THE PREPARATION OF HETEROCYCLIC SULFONAMIDE COMPOUNDS

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Page/Page column 23-24, (2009/02/11)

Methods for preparing compound of formula (I) are described, wherein R1-R3 are defined herein, as are methods for preparing the intermediates formed therein. Also described are methods for enantioselectively preparing a chiral compou

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