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benzyl (2S,5R,6R)-6-<(R)-1-hydroxyethyl>penicillanate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62263-79-0

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62263-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62263-79-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,6 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62263-79:
(7*6)+(6*2)+(5*2)+(4*6)+(3*3)+(2*7)+(1*9)=120
120 % 10 = 0
So 62263-79-0 is a valid CAS Registry Number.

62263-79-0Downstream Products

62263-79-0Relevant academic research and scientific papers

FROM PENICILLIN TO PENEM AND CARBAPENEM. II. SYNTHESIS OF 3,4-DISUBSTITUTED AZETIDINONE DERIVATIVES FROM 6,6-BIS(PHENYLSELENYL)PENICILLANATE

Hirai, Koichi,Iwano, Yuji,Fujimoto, Katsumi

, p. 4021 - 4024 (2007/10/02)

6,6-Bis(phenylselenyl)penicillanate 2a was converted into 6-1'-(R)-hydroxyethyl substituted penicillanate 5 in high yield.Compound 5 was deselenylated to 10.Oxidation, and then the basic epimerization of cis sulfone 11 gave trans sulfone derivative 12.The trans sulfone 12 was degraded to the monocyclic β-lactams 14, 15 which are important precursors for the carbapenem synthesis.

2-(Alkylthio)penem-3-carboxylic Acids. IV. Synthesis of (Hydroxyethyl)-azetidinone Precursors to 1-Thia Analogs of Thienamycin

Yoshida, Akira,Hayashi, Teruo,Takeda, Noriko,Oida, Sadao,Ohki, Eiji

, p. 2899 - 2909 (2007/10/02)

The synthesis of hydroxyethylazetidinone precursors to 1-thia analogs of thienamycin is described.An N-protected azetidinone 4 was hydroxyethylated via an aldol reaction to give four diastereomers 5-8, which were converted to the diastereomeric pair of racemic 8R and 8S trans azetidinones 9b and 10b.Stereochemical assignment was achieved by correlation of 9b with the optically active azetidinone 16 which was obtained from the hydroxyethylpenicillanate 14a with known stereochemistry.The optically active 8R and 8S azetidinones 16 and 27 were synthesized more efficiently starting from the penicillinderived bromo compound 19 in a series of steps including stereochemical inversion at the C-8 position.Keywords-- antibiotics; β-lactam; hydroxyethylazetidinones; aldol reaction; aluminium enolate of β-lactam; stereochemical inversion; triphenylphosphine/diethyl azodicarboxylate system; penicillin degradation

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