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7-Cyclohexyl-heptandiol-(1,4) is a complex organic compound with the molecular formula C13H24O2. It features a cyclohexane ring attached to a heptane chain, with two hydroxyl (-OH) groups located at the 1st and 4th carbon positions of the heptane chain. This molecule is characterized by its unique structure, which combines the properties of a cycloalkane with those of a diol. The presence of two hydroxyl groups endows it with potential reactivity in chemical synthesis, such as in the formation of esters, ethers, or other derivatives. The compound may have applications in the pharmaceutical, chemical, or materials science industries, where its specific structural features could be leveraged for the development of new products or processes.

2205-29-0

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2205-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2205-29-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2205-29:
(6*2)+(5*2)+(4*0)+(3*5)+(2*2)+(1*9)=50
50 % 10 = 0
So 2205-29-0 is a valid CAS Registry Number.

2205-29-0Downstream Products

2205-29-0Relevant academic research and scientific papers

Synthesis of γ-Lactones Utilizing Ketoacids and Trimethylsulfoxonium Iodide

Triandafillidi, Ierasia,Savvidou, Anatoli,Kokotos, Christoforos G.

, p. 5533 - 5537 (2019)

The Johnson-Corey-Chaykovsky epoxidation is one of the oldest methods for the synthesis of terminal epoxides from carbonyl compounds. Herein we present a simplified extension of the Johnson-Corey-Chaykovsky epoxidation, where ketoacids are employed as the substrates and commercially available trimethylsulfoxonium iodide is employed as the carbon-atom homologating reagent. A variety of lactones are produced in a single step in synthetically useful yields.

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