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4-Cyclohexyl-2-butynal is an organic compound with the molecular formula C10H14O. It is a colorless liquid with a strong, pungent odor. This aldehyde derivative features a cyclohexyl group attached to a butynal chain, which consists of a triple bond between two carbon atoms and a carbonyl group. The compound is used in the synthesis of various pharmaceuticals, agrochemicals, and fragrances due to its unique chemical structure and reactivity. It is also known for its potential applications in the production of specialty chemicals and materials. The compound's properties, such as its boiling point, solubility, and stability, make it a valuable intermediate in organic synthesis.

5962-80-1

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5962-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5962-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5962-80:
(6*5)+(5*9)+(4*6)+(3*2)+(2*8)+(1*0)=121
121 % 10 = 1
So 5962-80-1 is a valid CAS Registry Number.

5962-80-1Downstream Products

5962-80-1Relevant academic research and scientific papers

Palladium-catalyzed oxidative borylation of conjugated enynones through carbene migratory insertion: synthesis of furyl-substituted alkenylboronates

Ping, Yifan,Chang, Taiwei,Wang, Kang,Huo, Jingfeng,Wang, Jianbo

, p. 59 - 62 (2019)

A palladium-catalyzed oxidative borylation reaction of conjugated enynones is developed. This reaction represents a new method for the synthesis of furyl-substituted alkenylboronates. The reaction works well with a series of conjugated enynones. Boryl migratory insertion of the palladium carbene intermediate is proposed as the key step in these transformations.

Gold(I)-catalyzed, stereocontrolled enamide synthesis from primary amides and propargyl aldehydes using a tandem strategy

Kim, Sang Min,Lee, Dabon,Hong, Soon Hyeok

supporting information, p. 6168 - 6171 (2015/01/16)

A novel strategy for enamide synthesis from primary amides and propargyl aldehydes via Au(I)-catalyzed tandem amide addition and Meyer-Schuster rearrangement is described. In situ generated hemiaminals were successfully converted to the desired products u

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