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N-<(benzyloxy)carbonyl>-2-<2-(tert-butyldimethylsiloxy)ethyl>piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153108-98-6

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153108-98-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153108-98-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,0 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 153108-98:
(8*1)+(7*5)+(6*3)+(5*1)+(4*0)+(3*8)+(2*9)+(1*8)=116
116 % 10 = 6
So 153108-98-6 is a valid CAS Registry Number.

153108-98-6Relevant academic research and scientific papers

MYXOVIRUS THERAPEUTICS, COMPOUNDS, AND USES RELATED THERETO

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Page/Page column 4; 26, (2013/05/21)

This disclosure relates to antiviral compounds disclosed herein and uses related thereto. In certain embodiments, the disclosure relates to pharmaceutical compositions. Typically, the pharmaceutical composition comprises a compound of formula I: Formula I

Non-nucleoside inhibitors of the measles virus RNA-dependent RNA polymerase: Synthesis, structure-activity relationships, and pharmacokinetics

Ndungu, J. Maina,Krumm, Stefanie A.,Yan, Dan,Arrendale, Richard F.,Reddy, G. Prabhakar,Evers, Taylor,Howard, Randy,Natchus, Michael G.,Saindane, Manohar T.,Liotta, Dennis C.,Plemper, Richard K.,Snyder, James P.,Sun, Aiming

supporting information; experimental part, p. 4220 - 4230 (2012/06/30)

The measles virus (MeV), a member of the paramyxovirus family, is an important cause of pediatric morbidity and mortality worldwide. In an effort to provide therapeutic treatments for improved measles management, we previously identified a small, non-nucl

NEW BRADYKININ B1 ANTAGONISTS

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Page/Page column 35, (2008/12/08)

The invention relates to compounds of formula (I), wherein R1 to R5 and X1 to X4, n and m have the meaning as cited in the description and the claims. Said compounds are useful as Bradykinin B1 antagonists. The

Highly stereoselective total syntheses of (+)-allopumiliotoxins 267A and 339A via intramolecular nickel(II)/chromium(II)-mediated cyclization

Aoyagi, Sakae,Wang, Tzu-Chueh,Kibayashi, Chihiro

, p. 11393 - 11409 (2007/10/02)

Remarkably high regio- and stereoselective approaches for the syntheses of dendrobatid alkaloids (+)allopumiliotoxin 267A and 339A have been develop. As a model study for these alkaloids, we initially undertook intramolecular chromium(II)-mediated cycliza

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