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3-acetoxy-1-(1-acetoxy-cyclohexyl)-3-methyl-but-1-yne is a complex organic compound with the molecular formula C15H22O4. It features a cyclohexane ring with an acetoxy group attached to one carbon atom, and a but-1-yne chain with two acetoxy groups and a methyl group attached to the terminal carbon atom. 3-acetoxy-1-(1-acetoxy-cyclohexyl)-3-methyl-but-1-yne is characterized by its unique structure, which includes a cyclohexane ring and a but-1-yne chain, both of which are functionalized with acetoxy groups. The presence of these functional groups gives the compound specific reactivity and properties that can be exploited in various chemical reactions and applications. The compound's structure also suggests potential use in the synthesis of more complex molecules, particularly those involving the cyclohexane and acetylene moieties.

3036-48-4

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3036-48-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3036-48-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,3 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3036-48:
(6*3)+(5*0)+(4*3)+(3*6)+(2*4)+(1*8)=64
64 % 10 = 4
So 3036-48-4 is a valid CAS Registry Number.

3036-48-4Relevant academic research and scientific papers

Gold-Catalyzed stereocontrolled synthesis of 2,3-Bis(acetoxy)-1,3-dienes

Huang, Xiaogen,De Haro, Teresa,Nevado, Cristina

supporting information; experimental part, p. 5904 - 5908 (2010/03/03)

A 1,4-bis(propargyl acetates) undergo a highly selective tandem 1,2-/1,2-Bis(acetoxy) migration to give 2,3-Bis(acetoxy)-1,3-dienes, that, depending on the catalyst of choice,(1Z,3Z) or (1Z,3E and 1E,3Z)-1,3-dienes can be obtained in a stereocontrolled manner. It was found that the 1,2-Bis(acetoxy) migration was favored in all studied cases and no allene product was observed in the reaction mixtures. It was also found that more e sterically demanding substrate dramatically improved the selectivity thereby revealing the key role of sterics in the stereocontrol of these transformations. The results show that the choice of the acetoxy migrating first seemed to be of key importance and is determined both by the electronic character and sterical bulkiness of substituents at the propargylic position.

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