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2,3-dimethyl-3-(4-methylphenyl)-cyclopentanol is a complex organic compound with the molecular formula C15H22O. It features a cyclopentanol ring, which is a five-membered ring with a hydroxyl group (-OH) attached to one of the carbon atoms. The structure is further characterized by two methyl groups (-CH3) at the 2nd and 3rd positions of the cyclopentane ring, and a 4-methylphenyl group attached to the 3rd carbon. The 4-methylphenyl group itself is a benzene ring with a methyl group at the 4th position. 2,3-dimethyl-3-(4-methylphenyl)-cyclopentanol is likely to be a colorless liquid with a distinct aroma, and it may have applications in the synthesis of pharmaceuticals, fragrances, or other specialty chemicals due to its unique structure and functional groups.

4608-43-9

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4608-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4608-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4608-43:
(6*4)+(5*6)+(4*0)+(3*8)+(2*4)+(1*3)=89
89 % 10 = 9
So 4608-43-9 is a valid CAS Registry Number.

4608-43-9Relevant academic research and scientific papers

Unified approach to the sesquiterpenoids, lauranes and cyclolauranes: Total synthesis of (±)-isolaurene

Niyogi,Khatua, Arindam,Bisai, Vishnumaya

, (2019/07/23)

A general approach to the total synthesis of sesquiterpene, isolaurene (1a) and cyclolaurene (2a) is featured from commercially available 3-methyl cyclopenten-2-one. The strategy includes a Stork-Danheiser sequence concomitant with a Ni(II)-catalyzed conj

Lithium-liquid ammonia mediated carbocyclisation of δ,ε- unsaturated esters: Annulation of cyclopentanones

Srikrishna,Ramasastry

, p. 379 - 382 (2007/10/03)

Lithium-liquid ammonia mediated carbanion cyclisation of δ,ε-unsaturated esters leading to cyclopentanes, fused as well as spiro, via annulation is described.

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