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1,2-Cyclohexanediol, 1-ethynyl- (6CI,7CI,8CI,9CI) is an organic compound with the chemical formula C8H10O2. It is a derivative of cyclohexane, featuring a diol functional group at the 1,2-positions and an ethynyl group at the 1-position. 1,2-Cyclohexanediol, 1-ethynyl- (6CI,7CI,8CI,9CI) is characterized by its unique structure, which combines the properties of a cyclohexane ring with the reactivity of a diol and an alkyne. It is used in the synthesis of various organic compounds and can be found in research and industrial applications, particularly in the pharmaceutical and chemical industries. The compound's unique structure and reactivity make it a valuable intermediate in the preparation of complex molecules and functional materials.

7312-60-9

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7312-60-9 Usage

Derivative

Cyclohexanediol

Functional group

Ethynyl group (a triple-bonded carbon atom)

Usage

a. Organic synthesis
b. Building block in pharmaceuticals and agrochemicals production
c. Research and development for new chemical compounds
d. Manufacturing of specialty chemicals
e. Flavors and fragrances industry

Unique properties

a. Unique molecular structure
b. Potential applications in various industries due to its properties

Check Digit Verification of cas no

The CAS Registry Mumber 7312-60-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7312-60:
(6*7)+(5*3)+(4*1)+(3*2)+(2*6)+(1*0)=79
79 % 10 = 9
So 7312-60-9 is a valid CAS Registry Number.

7312-60-9Relevant academic research and scientific papers

Unexpected diels-Alder/carbonyl-ene cascade toward the biomimetic synthesis of chloropupukeananin

Suzuki, Takahiro,Miyajima, Yuria,Suzuki, Kaname,Iwakiri, Kanako,Koshimizu, Masaki,Hirai, Go,Sodeoka, Mikiko,Kobayashi, Susumu

supporting information, p. 1748 - 1751 (2013/07/05)

The biomimetic synthesis of the advanced model compound of chloropupukeananin has been achieved. The present synthesis features an unexpected enantiomer-differentiating Diels-Alder/carbonyl-ene cascade under high-pressure conditions and a base-promoted migration of the salicyl group.

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