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Heptanoic acid cyclohexylmethyl ester is an organic compound with the chemical formula C14H24O2. It is an ester derived from heptanoic acid and cyclohexylmethyl alcohol. This colorless liquid has a fruity, floral, and slightly green odor, making it a valuable component in the fragrance industry. It is used in the production of perfumes, cosmetics, and other scented products due to its pleasant aroma. The compound is also known for its low toxicity and is considered safe for use in these applications.

2890-69-9

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2890-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2890-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2890-69:
(6*2)+(5*8)+(4*9)+(3*0)+(2*6)+(1*9)=109
109 % 10 = 9
So 2890-69-9 is a valid CAS Registry Number.

2890-69-9Downstream Products

2890-69-9Relevant academic research and scientific papers

Ruthenium Complex Catalyzed Intermolecular Hydroacylation and Transhydroformylation of Olefins with Aldehydes

Kondo, Teruyuki,Akazome, Motohiro,Tsuji, Yasushi,Watanabe, Yoshihisa

, p. 1286 - 1291 (2007/10/02)

Low-valent ruthenium complexes such as dodecacarbonyltriruthenium (Ru3(CO)12), (η4-1,5-cyclooctadiene)(η6-1,3,5-cyclooctatriene)ruthenium (Ru(COD)(COT)) and bis(η5-cyclooctadienyl)ruthenium showed high catalytic activity for the intermolecular hydroacylation of olefins with various aromatic and heteroaromatic aldehydes at 180-200 deg C for 24-48 h under an initial carbon monoxide pressure of 20 kg cm-2 to give unsymmetric ketones in moderate to good yields.In the reaction of 2-thiophenecarbaldehyde with cyclohexene, cyclohexyl 2-thienyl ketone was obtained in 62 percent yield.On the other hand, when the aliphatic aldehyde, heptanal, was treated with cyclohexene, the corresponding ketone was not obtained at all, and a transhydroformylation reaction proceeded; i.e., the formyl group of heptanal was apparently transformed to cyclohexene to give cyclohexanecarbaldehyde in 29 percent yield, together with their Tishchenko-type reaction products.

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