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benzyl (-)-(2S,5S,6R)-3,3-dimethyl-7-oxo-6-phthalimido-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59034-30-9

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59034-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59034-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,3 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 59034-30:
(7*5)+(6*9)+(5*0)+(4*3)+(3*4)+(2*3)+(1*0)=119
119 % 10 = 9
So 59034-30-9 is a valid CAS Registry Number.

59034-30-9Downstream Products

59034-30-9Relevant academic research and scientific papers

Asymmetric synthesis of new β-lactam lipopeptides as bacterial signal peptidase i inhibitors

Crauste, Celine,Froeyen, Matheus,Anne, Jozef,Herdewijn, Piet

experimental part, p. 3437 - 3449 (2011/09/12)

The transmembrane bacterial enzyme, signal peptidase I, is recognized as being a promising target for reducing the emergence of drug resistance. The asymmetric synthesis and the biological evaluation of original β-lactam lipopeptides have been performed t

Syntheses of (6S)-cephalosporins from 6-aminopenicillanic acid

Fekner, Tomasz,Baldwin, Jack E,Adlington, Robert M,Jones, Timothy W,Prout, C.Keith,Schofield, Christopher J

, p. 6053 - 6074 (2007/10/03)

Two practical routes to (6S,7S)-cephalosporins from 6-aminopenicillanic acid (6-APA) are described. In the first, 6-APA was converted to (2S,4S,5S,6S)-penicillin sulfoxide 49, which underwent Morin ring expansion to a protected (6S,7S)-cephem 50. In the s

Syntheses of (6S,7S)- and (6S,7R)-deacetoxycephalosporanic acids from 6-aminopenicillanic acid

Fekner, Tomasz,Baldwin, Jack E.,Adlington, Robert M.,Schofield, Christopher J.

, p. 1989 - 1990 (2007/10/03)

Two practical (i.e. applicable to multigram scale synthesis) approaches to (6S,7S)-cephalosporins (i.e. the enantiomers of naturally occuring cephalosporins) and the (6S)-epimers of cephalosporins from readily available (2S,5R,6R)-6-aminopenicillanic acid

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