697762-66-6 Usage
General Description
The chemical "1-((S)-1-tert-butyldiMethylsilyloxyMethyl-2-Methylpropyl)-6-(3-chloro-2-fluorobenzyl)-7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester" is a complex compound with a long and specific name. It is an ethyl ester derivative of a quinolone antibiotic, with a molecular structure that includes a fluoroquinolone core, a tert-butyldimethylsilyloxy group, and a chlorofluorobenzyl group. It is likely to have antibacterial properties due to its similarity to other quinolone antibiotics, and the specific chemical modifications may affect its pharmacokinetics and potency. 1-((S)-1-tert-butyldiMethylsilyloxyMethyl-2-Methylpropyl)-6-(3-chloro-2-fluorobenzyl)-7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester has the potential to be important for pharmaceutical research and the development of new antibiotics.
Check Digit Verification of cas no
The CAS Registry Mumber 697762-66-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,7,6 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 697762-66:
(8*6)+(7*9)+(6*7)+(5*7)+(4*6)+(3*2)+(2*6)+(1*6)=236
236 % 10 = 6
So 697762-66-6 is a valid CAS Registry Number.
697762-66-6Relevant articles and documents
AN IMPROVED PROCESS FOR THE PREPARATION OF ELVITEGRAVIR
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, (2011/02/24)
The present invention relates to improved process for the preparation of elvitegravir (12), wherein the compound of formula (6) is protected with suitable protecting agents and further reacted with formula (9) in the presence of tetrakis(triphenylphosphin
Novel HIV-1 integrase inhibitors derived from quinolone antibiotics
Sato, Motohide,Motomura, Takahisa,Aramaki, Hisateru,Matsuda, Takashi,Yamashita, Masaki,Ito, Yoshiharu,Kawakami, Hiroshi,Matsuzaki, Yuji,Watanabe, Wataru,Yamataka, Kazunobu,Ikeda, Satoru,Kodama, Eiichi,Matsuoka, Masao,Shinkai, Hisashi
, p. 1506 - 1508 (2007/10/03)
The viral enzyme integrase is essential for the replication of human immunodeficiency virus type 1 (HIV-1) and represents a remaining target for antiretroviral drugs. Here, we describe the modification of a quinolone antibiotic to produce the novel integr