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(S)-methyl 3-(5-bromo-2,4-difluorophenyl)-3-((R)-1,1-dimethylethylsulfinamido)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1194044-31-9

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1194044-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1194044-31-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,0,4 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1194044-31:
(9*1)+(8*1)+(7*9)+(6*4)+(5*0)+(4*4)+(3*4)+(2*3)+(1*1)=139
139 % 10 = 9
So 1194044-31-9 is a valid CAS Registry Number.

1194044-31-9Relevant academic research and scientific papers

Synthesis of β-disubstituted β-amino isoxazolyl ketones by addition of ketimines with isoxazolyl methyl ketone enolates

Guernon, Jason,Marcin, Lawrence,Higgins, Mendi,Yang, Fukang,Shi, Jianliang,Snyder, Lawrence,Thompson, Lorin A.,Wu, Yong-Jin

, p. 2134 - 2137 (2015/03/18)

A series of β-disubstituted N-sulfinyl β-amino isoxazolyl ketones has been prepared by addition of tert-butanesulfinyl ketimines with the n-BuLi-generated enolates of isoxazolyl methyl ketones.

4,6-DIARYLAMINOTHIAZINES AS BACE1 INHIBITORS AND THEIR USE FOR THE REDUCTION OF BETA-AMYLOID PRODUCTION

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Page/Page column 39; 40, (2014/07/08)

Compounds of formula (I), including pharmaceutically acceptable salts thereof, are set forth herein: (I) wherein R1 and R2 are independently hydrogen, or -CH3; or R1 and R2 can join together in a ring by adding -(CH2)4-; R3 is hydrogen or C1-C3 al-kyl; Y and Z are independently a C6-C10- aryl group or a 5-10 membered heterocyclic group which can be further substituted with from 0-3 substituents selected from the group of halogen, hydroxy, amino, C1-4 alkylamino, C1-4 dialkylamino, halo C1-4 alkyl, CN, C1-C6, alkyl or cycloalkyl, C1-C6 alkoxy, -C=OC1-4 alkyl, -SO2C1-4 alkyl, and C2-C4 alkynyl; A is selected from the group of phenyl, ben-zyl, oxazolyl, thiazolyl, isoxazolyl, imidazolyl, pyrazolyl, pyridyl, pyrimidinyl, and pyrazinyl groups which can be further substituted with from 0-3 substituents selected from the group of halogen, hydroxy, amino, C1-4 alkylamino, C1-4 dialkylamino, haloC1-4 alkyl, hydroxyC1-6 alkyl, CN, C1-C6 alkyl or cycloalkyl, C1-C6 alkoxy, and C2-C4 alkynyl; L is -NHCO-, or is a single bond; and L and Z to-gether can be absent

BACE INHIBITORS

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Page/Page column 8-9, (2009/12/02)

The present invention provides BACE inhibitors of Formula I: methods for their use, and intermediates and methods for their preparation.

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