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Benzenepentanoic acid, a-diazo-b-oxo-, 2-(trimethylsilyl)ethyl ester is a complex organic compound with the chemical formula C15H24NO4Si. It is a derivative of benzenepentanoic acid, featuring a diazo group (-N2) and an oxo group (-O) in the beta position relative to the carboxylic acid functional group. The molecule also includes a trimethylsilylethyl ester group, which is attached to the carboxylic acid, providing a unique structure with potential applications in chemical synthesis and research. Benzenepentanoic acid, a-diazo-b-oxo-, 2-(trimethylsilyl)ethyl ester is characterized by its ester functionality, which can participate in various chemical reactions, and its trimethylsilyl group, which can influence the reactivity and stability of the molecule.

113995-19-0

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113995-19-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113995-19-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,9,9 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113995-19:
(8*1)+(7*1)+(6*3)+(5*9)+(4*9)+(3*5)+(2*1)+(1*9)=140
140 % 10 = 0
So 113995-19-0 is a valid CAS Registry Number.

113995-19-0Upstream product

113995-19-0Relevant academic research and scientific papers

INTERMOLECULAR RHODIUM CARBENOID INSERTIONS INTO THE N-H BOND OF β-LACTAMS. SYNTHESIS OF O-2-ISOCEPHEMS

Hrytsak, Michael,Durst, Tony

, p. 2393 - 2409 (2007/10/02)

A new, convergent synthesis of O-2-isocephems is reported.Rhodium carbenoid insertion of α-diazo-β-ketoesters into the N-H bond of a preformed β-lactam, followed by cyclization of the resulting enol-alcohols by Mitsunobu reaction gives the title compounds

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