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methyl 2-(cyclohex-1-en-1-yl)-2-oxoacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65499-26-5

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65499-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65499-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,4,9 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65499-26:
(7*6)+(6*5)+(5*4)+(4*9)+(3*9)+(2*2)+(1*6)=165
165 % 10 = 5
So 65499-26-5 is a valid CAS Registry Number.

65499-26-5Relevant academic research and scientific papers

3-Hydroxy-2-oxo-1-oxaspiro[4.5]-dec-3-ene, a new inhibitor of lactate dehydrogenase

Kato, Yasuo

, p. 4809 - 4812 (1995)

Methods for the synthesis of the spirolactone [3-hydroxy-2-oxo-1-oxaspiro[4.5]-dec-3-ene, 3] and the sodium salts of two new α-keto acids [(1-cyclohexenyl)glyoxylate 1, β-(1-hydroxycyclohexane)pyruvate (enol form, 2)] are described. These compounds are ex

Synthesis and biological activity of new C-6 and C-7 substituted vinyloxyimino-penicillins and -cephalosporins

Fell, Stephen C. M.,Pearson, Michael J.,Burton, George,Elder, John S.

, p. 1483 - 1494 (2007/10/02)

The Wittig reaction has been successfully utilized in the preparation of a number of substituted α-vinyloxyiminoacetic acids, the subsequent coupling of which to the 6-APA and 7-ACA nuclei has provided a range of potent β-lactam antibiotics.Development of other procedures for olefin synthesis has broadened the scope, with the preparation of a range of alkenyl-, cycloalkenyl- and arylvinyl-oxyiminoacetamidopenicillins and cephalosporins.

INTRAMOLECULAR NITRONE-ALKYNE CYCLOADDITION

Kang, Han-Young,Cho, Yong Seo,Koh, Hun Yeong,Chang, Moon Ho

, p. 2779 - 2782 (2007/10/02)

It is demonstrated that the cycloaddition of a nitrone to an alkyne is facile when the length of the tether connecting the two reacting sites is appropriate.The resulting cycloaddition products, isoxazolidines can be further converted to 3-hyd

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