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175853-53-9

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175853-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175853-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,8,5 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 175853-53:
(8*1)+(7*7)+(6*5)+(5*8)+(4*5)+(3*3)+(2*5)+(1*3)=169
169 % 10 = 9
So 175853-53-9 is a valid CAS Registry Number.

175853-53-9Relevant academic research and scientific papers

THERAPEUTIC COMPOUNDS

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Page/Page column 32, (2017/08/22)

The present invention relates to compounds that are antagonists of the orexin-1 receptor. The compounds have the structural formula (I) defined herein. The present invention also relates to processes for the preparation of these compounds, to pharmaceutical compositions comprising them, and to their use in the treatment of diseases or disorders associated with orexin-1 receptor activity.

'N-stereogenic quaternary ammonium salts' from L-amino acids: Synthesis, separation, and absolute configuration

Wu, Hua-Fang,Lin, Wen-Bin,Xia, Li-Zi,Luo, Ying-Gang,Chen, Xiao-Zhen,Li, Guo-You,Zhang, Guo-Lin,Pan, Xin-Fu

experimental part, p. 677 - 688 (2009/08/08)

Diastereoisomeric linear and cyclic 'N-chiral quaternary ammonium salts' (QASs) were efficiently synthesized from corresponding L-amino acids in high yields. The diastereoisomers of each pair of 'N-chiral QASs' were successfully separated. The absolute configurations of these QASs were determined predominately by X-ray single-crystal analysis. The 1H-NMR data of 'N-chiral QASs' provided characteristic information on the configuration of the N-chiral center. 'N-Chiral QASs' exemplified by [N(R)]-2a and [N(S)]-2a are stable in protic and aprotic solvents within a broad pH and temperature range.

Photoinduced electron transfer (PET) promoted oxidative activation of 1- (N-benzyl-N-methylglycyl)-(S)-prolinol: Development of novel strategies towards enantioselective syntheses of α-amino acids, their N-methyl derivatives and α-hydroxy acids employing

Pandey, Ganash,Das, Parthasarathi,Reddy, P. Yella

, p. 657 - 664 (2007/10/03)

PET activation of 1-(N-benzyl-N-methylglycyl)-(S)-prolinol (1) in dry acetonitrile, utilizing 1,4-dicyanonaphthalene (DCN) as a light-harvesting electron-acceptor and methyl viologen (MV++) as an electron-transfer mediator, leads to the formati

Chirale Boran-Amin-Addukte in der asymmetrischen Synthese: Alkylierung von Alaninderivaten

Ferey, Vincent,Toupet, Loic,Gall, Thierry Le,Mioskowski, Charles

, p. 475 - 477 (2007/10/03)

Keywords: Aminosaeuren; Asymmetrische Synthesen; Borverbindungen; Chiralitaet; Enolate

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