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(-)-2,10-Epoxypinane is a naturally occurring sesquiterpene compound, characterized by a unique seven-membered ring structure and an epoxy group at the 2,10 positions. It is found in various plant species, particularly in the essential oils of some conifers, and is known for its potential biological activities, such as antimicrobial and anti-inflammatory properties. The compound's stereochemistry, with a negative configuration at the 2,10 positions, is crucial for its specific interactions with biological targets. Research on (-)-2,10-epoxypinane and its derivatives may lead to the development of new pharmaceuticals or agrochemicals, highlighting the importance of studying such natural products for their potential applications in various fields.

875-08-1

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875-08-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 875-08-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 875-08:
(5*8)+(4*7)+(3*5)+(2*0)+(1*8)=91
91 % 10 = 1
So 875-08-1 is a valid CAS Registry Number.

875-08-1Upstream product

875-08-1Relevant academic research and scientific papers

Cyclobutane Ring Opening of Pin-2(10)-ene with Mercury(II) Salts. A New, High-yield Synthesis of p-Mentha-1,8-dien-7-ol

Bluthe, Norbert,Ecoto, Jules,Fetizon, Marcel,Lazare, Sylvain

, p. 1747 - 1751 (2007/10/02)

The nucleophilic attack of pin-2(10)-ene-mercury(II) complex systems by water results in the opening of the four-membered ring leading to an allylic organomercury(II) derivative (11) with the p-menthane skeleton.This intermediate can be reduced by hydride to p-menth-1(2)-en-8-ol (6a) or can undergo an in situ SE2' elimination yielding p-menth-1(7)-en-8-ol (9a), in high yields. (-)-2,10-Epoxypinane (15) reacts with mercury(II) salts at room temperature, giving the diol (16) in a quantitative yield.Compound (16) is a suitable intermediate for convenient preparation of p-mentha-1,8-dien-7-ol (17) and its derivatives.

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