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Benzyl α-cyano-α-oximinoacetate is a chemical compound with the molecular formula C11H10N2O2. It is a derivative of α-cyanoacetate, featuring a benzyl group attached to the α-carbon, and an oxime group at the α-carbon as well. benzyl α-cyano-α-oximinoacetate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. Its structure provides a platform for further chemical modifications, making it a valuable building block in organic chemistry. The compound's properties, such as its reactivity and stability, are influenced by the presence of the cyano group and the oxime functionality, which can participate in various chemical reactions, including cycloadditions and rearrangements.

718-31-0

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718-31-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 718-31-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 718-31:
(5*7)+(4*1)+(3*8)+(2*3)+(1*1)=70
70 % 10 = 0
So 718-31-0 is a valid CAS Registry Number.

718-31-0Upstream product

718-31-0Relevant academic research and scientific papers

Enantiospecific synthesis of carbocyclic aminoimidazole carboxamide ribonucleotide (C-AICAR), succinoaminoimidazole carboxamide ribonucleotide (C-SAICAR), and a new intermediate for SAICAR analogs

Schmitt,Caperelli

, p. 1929 - 1945 (2007/10/02)

The (-)-enantiomer of the carbocyclic analogs of aminoimidazole carboxamide ribonucleotide (C-AICAR, 7), and succinoaminoimidazole carboxamide ribonucleotide (C-SAICAR, 14) have been prepared. En route, a new intermediate (19) for the preparation of SAICAR analogs was developed.

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