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(1S)-2-isopropylidene-5t-methyl-cyclopentane-r-carbaldehyde is a complex organic compound with a unique molecular structure. It is a chiral molecule, denoted by the (1S) configuration, which indicates the spatial arrangement of atoms around the chiral center. The compound features a cyclopentane ring, which is a five-membered ring structure, with an isopropylidene group (a three-carbon chain with two methyl groups) attached to the second carbon. Additionally, it has a methyl group (a single carbon atom with three hydrogen atoms) at the fifth position of the cyclopentane ring. The molecule is further characterized by a carbonyl group (C=O) at the first position, which classifies it as a carbaldehyde. This carbonyl group is crucial for its reactivity and potential applications in organic synthesis, particularly in the formation of various derivatives and its role as a precursor in the synthesis of more complex molecules.

60586-78-9

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60586-78-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60586-78-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,8 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60586-78:
(7*6)+(6*0)+(5*5)+(4*8)+(3*6)+(2*7)+(1*8)=139
139 % 10 = 9
So 60586-78-9 is a valid CAS Registry Number.

60586-78-9Downstream Products

60586-78-9Relevant academic research and scientific papers

Studies on Horner-Wadsworth-Emmons reaction in base sensitive ketones: Synthesis of (-)-mitsugashiwalactone and formal synthesis of (+)-iridomyrmecin, (-)-isoiridomyrmecin and (+)-teucriumlactone

Nangia,Prasuna

, p. 3435 - 3450 (1996)

The effect of different bases in promoting Horner-Wadsworth-Emmons (HWE) reaction on enolisable cyclopentanones is investigated. NaH is found to be suitable for the intermolecular reaction and DBU/LiCl is optimal for the intramolecular variation. The HWE approach is employed for the enantioselective synthesis of iridoid cyclopentapyranones of type-I (4, 16, 52) and type-II (5, 36).

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