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α-[2-Chloro-1-hydroxy-1-(hydroxyMethyl)ethyl]-7-oxo-3-phenyl-4-oxa-2,6-diazabicyclo[3.2.0]hept-2-ene-6-acetic Acid DiphenylMethyl Ester is a complex organic compound characterized by its unique molecular structure. It is an intermediate in the synthesis of oxacephem derived beta-lactam antibiotics, which are known for their effectiveness against gram-positive bacteria.

68313-69-9

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68313-69-9 Usage

Uses

Used in Pharmaceutical Industry:
α-[2-Chloro-1-hydroxy-1-(hydroxyMethyl)ethyl]-7-oxo-3-phenyl-4-oxa-2,6-diazabicyclo[3.2.0]hept-2-ene-6-acetic Acid DiphenylMethyl Ester is used as an intermediate in the synthesis of oxacephem derived beta-lactam antibiotics for their effectiveness against gram-positive bacteria. This application is due to its role in the development of new antibiotics that can combat resistant strains of bacteria, which is a significant concern in the medical field.

Check Digit Verification of cas no

The CAS Registry Mumber 68313-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,1 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68313-69:
(7*6)+(6*8)+(5*3)+(4*1)+(3*3)+(2*6)+(1*9)=139
139 % 10 = 9
So 68313-69-9 is a valid CAS Registry Number.

68313-69-9Relevant academic research and scientific papers

CONVENIENT SYNTHESIS OF 3'-SUBSTITUTED METHYL 7α-METHOXY-1-OXACEPHEMS

Aoki, Tsutomu,Yoshioka, Mitsuru,Kamata, Susumu,Konoike, Toshiro,Haga, Nobuhiro,Nagata, Wataru

, p. 409 - 413 (2007/10/02)

A convenient synthesis of the title compounds 1 is achieved by formation of glycols 3, 12, 13 and 14 or chlorohydrins 6 from epioxazolines having pertinent allylic substituents, followed by stereoselective, intramolecular etherification to 4, 7, 15, 16 an

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