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3-Cyclohexylidene-propan-1-ol, also known as 3-cyclohexylidene-1-propananol or 3-cyclohexylidenepropan-1-ol, is an organic compound with the molecular formula C9H16O. It is a colorless liquid with a density of 0.96 g/cm3 and a boiling point of 220°C. 3-Cyclohexylidene-propan-1-ol is characterized by a cyclohexane ring fused to a propanol group, with the hydroxyl group (-OH) attached to the third carbon of the propane chain. 3-Cyclohexylidene-propan-1-ol is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential applications in the fragrance industry due to its unique scent profile. The compound is typically synthesized through various chemical reactions, such as the condensation of cyclohexanone with propionaldehyde in the presence of a catalyst.

4361-24-4

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4361-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4361-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,6 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4361-24:
(6*4)+(5*3)+(4*6)+(3*1)+(2*2)+(1*4)=74
74 % 10 = 4
So 4361-24-4 is a valid CAS Registry Number.

4361-24-4Downstream Products

4361-24-4Relevant academic research and scientific papers

Chiral Selenide-Catalyzed Enantioselective Allylic Reaction and Intermolecular Difunctionalization of Alkenes: Efficient Construction of C-SCF3 Stereogenic Molecules

Liu, Xiang,Liang, Yaoyu,Ji, Jieying,Luo, Jie,Zhao, Xiaodan

supporting information, p. 4782 - 4786 (2018/04/17)

New approaches for the synthesis of enantiopure trifluoromethylthiolated molecules by chiral selenide-catalyzed allylic trifluoromethylthiolation and intermolecular difunctionalization of unactivated alkenes are disclosed. In these transformations, functi

REDUCTION OF ALLENIC ALCOHOLS BY SACCHAROMYCES CEREVISIAE

Gil, Gerard,Ferre, Elisee,Barre, Michael,le Petit, Jean

, p. 3797 - 3798 (2007/10/02)

α-Allenic alcohols are reduced by Saccharomyces cerevisiae into the corresponding β-ethylenic alcohols, whereas β-allenic alcohols undergo an isomerization leading to their γ-acetylenic counterparts.

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