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2-(4-bromo-2,6-dimethylphenyl)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943741-22-8

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943741-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943741-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,7,4 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 943741-22:
(8*9)+(7*4)+(6*3)+(5*7)+(4*4)+(3*1)+(2*2)+(1*2)=178
178 % 10 = 8
So 943741-22-8 is a valid CAS Registry Number.

943741-22-8Relevant academic research and scientific papers

Neutral macrocyclic factor VIIa inhibitors

Wurtz, Nicholas R.,Parkhurst, Brandon L.,DeLucca, Indawati,Glunz, Peter W.,Jiang, Wen,Zhang, Xiaojun,Cheney, Daniel L.,Bozarth, Jeffrey M.,Rendina, Alan R.,Wei, Anzhi,Harper, Tim,Luettgen, Joseph M.,Wu, Yiming,Wong, Pancras C.,Seiffert, Dietmar A.,Wexler, Ruth R.,Priestley, E. Scott

, p. 2650 - 2654 (2017/05/29)

Factor VIIa (FVIIa) inhibitors have shown strong antithrombotic efficacy in preclinical thrombosis models with limited bleeding liabilities. Discovery of potent, orally active FVIIa inhibitors has been largely unsuccessful due to the requirement of a basi

Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A-C

Ueda, Yoshihiro,Furuta, Takumi,Kawabata, Takeo

supporting information, p. 11966 - 11970 (2015/10/12)

The first total syntheses of multifidosides A-C have been achieved. The synthetic strategy is characterized by catalytic site-selective acylation of unprotected glycoside precursors in the final stage of the synthesis. High functional-group tolerance of the site-selective acylation, promoted by an organocatalyst, enabled the conventionally difficult molecular transformation in a predictable and reliable manner. An advantage of this strategy is to avoid the risks of undesired side reactions during the removal of the protecting groups at the final stage of the total synthesis.

MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS

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Page/Page column 123, (2008/12/07)

The present invention relates generally to novel macrocycles of Formula (I) or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof, wherein the variables A, B, C, D, L, M, W, Z1, Z2, Z3, Z4, R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

MACROCYCLIC FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS

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Page/Page column 151, (2008/06/13)

The present invention relates generally to novel macrocycles of Formula (I): or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, thereof, wherein the variables A, B, L, M, W, Z, R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 are as defined herein. These compounds are selective inhibitors of the serine protease coagulation factor VIIa which can be used as medicaments.

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