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3-(3-Butenyl)-2-methyl-4-oxo-2-cyclohexen-1-carbonsaeure-ethylester, also known as ethyl 3-(3-butenyl)-2-methyl-4-oxo-2-cyclohexen-1-carboxylate, is a complex organic compound with the molecular formula C13H18O3. It is a derivative of cyclohexen-1-carboxylic acid, featuring a 3-butenyl group, a methyl group, and an ethyl ester functional group. 3-(3-Butenyl)-2-methyl-4-oxo-2-cyclohexen-1-carbonsaeure-ethylester is characterized by its unique structure, which includes a cyclohexenone ring with a double bond and a carbonyl group, making it a potential intermediate in the synthesis of various pharmaceuticals, fragrances, and other specialty chemicals. Its chemical properties and reactivity are influenced by the presence of these functional groups, which can participate in a range of chemical reactions, such as esterification, oxidation, and reduction.

4994-08-5

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4994-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4994-08-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4994-08:
(6*4)+(5*9)+(4*9)+(3*4)+(2*0)+(1*8)=125
125 % 10 = 5
So 4994-08-5 is a valid CAS Registry Number.

4994-08-5Relevant academic research and scientific papers

THE INFLUENCE OF HYDROGEN BONDING ON THE SOLVOLYTIC REACTIVITY OF NICOTINATES IN FLUORINATED ALCOHOLS

Jursic, Branko,Sunko, Dionis E.,Ladika, Mladen

, p. 4367 - 4376 (1987)

A systematic investigation of solvolytic reactivities of allylic and benzylic nicotinates and their N-methylated derivatives in 80percent EtOH, 97percent TFE and 97percent HFIP was undertaken.The nicotinates in 97percent HFIP are slightly more reactive th

Stereocontrol in a combined allylic azide rearrangement and intramolecular schmidt reaction

Liu, Ruzhang,Gutierrez, Osvaldo,Tantillo, Dean J.,Aube, Jeffrey

supporting information; experimental part, p. 6528 - 6531 (2012/06/15)

Pre-equilibration of an interconverting set of isomeric allylic azides is coupled with an intramolecular Schmidt reaction to afford substituted lactams stereoselectively. The effect of substitution and a preliminary mechanistic study are reported. The syn

Solvolysis of 2-Alkenyl-2-cyclohexenyl p-Nitrobenzoates

Ladika, Mladen,Sunko, Dionis E.

, p. 4544 - 4548 (2007/10/02)

In an attempt to study possible ?-participation in allyl derivatives, 2-alkenyl-3-methyl-2-cyclohexenyl p-nitrobenzoates 6 and 7 were solvolyzed in 97 wt percent trifluoroethanol and 80 vol percent ethanol.These esters show in both solvents a solvolysis r

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