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1401065-46-0

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1401065-46-0 Usage

General Description

(S)-4-benzyl-3-(5,5,5-trifluoropentanoyl)oxazolidin-2-one is a chemical compound with a unique structure that includes a benzyl group and a trifluoropentanoyl group bound to an oxazolidin-2-one ring. (S)-4-benzyl-3-(5,5,5-trifluoropentanoyl)oxazolidin-2-one is a chiral molecule, meaning it has a non-superimposable mirror image, and is commonly used in organic chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals. The presence of the trifluoropentanoyl group gives the compound unique properties, such as increased hydrophobicity and potential for use as a bioactive molecule. Due to its versatile structure and potential applications, (S)-4-benzyl-3-(5,5,5-trifluoropentanoyl)oxazolidin-2-one is a valuable compound in chemical and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 1401065-46-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,6 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1401065-46:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*6)+(3*5)+(2*4)+(1*6)=100
100 % 10 = 0
So 1401065-46-0 is a valid CAS Registry Number.

1401065-46-0Downstream Products

1401065-46-0Relevant articles and documents

Discovery of clinical candidate BMS-906024: A potent pan-notch inhibitor for the treatment of leukemia and solid tumors

Gavai, Ashvinikumar V.,Quesnelle, Claude,Norris, Derek,Han, Wen-Ching,Gill, Patrice,Shan, Weifang,Balog, Aaron,Chen, Ke,Tebben, Andrew,Rampulla, Richard,Wu, Dauh-Rurng,Zhang, Yingru,Mathur, Arvind,White, Ronald,Rose, Anne,Wang, Haiqing,Yang, Zheng,Ranasinghe, Asoka,D'Arienzo, Celia,Guarino, Victor,Xiao, Lan,Su, Ching,Everlof, Gerry,Arora, Vinod,Shen, Ding Ren,Cvijic, Mary Ellen,Menard, Krista,Wen, Mei-Li,Meredith, Jere,Trainor, George,Lombardo, Louis J.,Olson, Richard,Baran, Phil S.,Hunt, John T.,Vite, Gregory D.,Fischer, Bruce S.,Westhouse, Richard A.,Lee, Francis Y.

supporting information, p. 523 - 527 (2015/05/27)

Structure-activity relationships in a series of (2-oxo-1,4-benzodiazepin-3-yl)-succinamides identified highly potent inhibitors of γ-secretase mediated signaling of Notch1/2/3/4 receptors. On the basis of its robust in vivo efficacy at tolerated doses in

ALKYL, FLUOROALKYL-1,4-BENZODIAZEPINONE COMPOUNDS

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Paragraph 00250; 00251, (2014/04/04)

Disclosed are compounds of Formula (I) and/or salts thereof: (I) wherein: R1 is CH2CH2CF3; R2 is CH2(cyclopropyl), CH(CH3)(cyclopropyl), or CH2CH2CH3/

FLUOROALKYL AND FLUOROCYCLOALKYL 1,4-BENZODIAZEPINONE COMPOUNDS AS NOTCH|INHIBITORS

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Paragraph 00172, (2014/04/04)

Disclosed are compounds of Formula (I): (Formula (I)) wherein: R1 is -CH2CH2CF3; R2 is -CH2CH2CH2F, -CH2CF2CH3, -CH2CH

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