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Δ8(9)-Pimaradiene is a naturally occurring diterpene compound, characterized by its unique bicyclic structure. It is found in various plants, particularly in the resin of certain conifers, and is known for its potential biological activities. Δ8(9)-pimaradiene has been studied for its anti-inflammatory, antimicrobial, and anticancer properties, making it a subject of interest in pharmaceutical research. Δ8(9)-Pimaradiene's chemical structure features a double bond between carbons 8 and 9, which contributes to its reactivity and potential therapeutic applications.

18319-61-4

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18319-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18319-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,1 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18319-61:
(7*1)+(6*8)+(5*3)+(4*1)+(3*9)+(2*6)+(1*1)=114
114 % 10 = 4
So 18319-61-4 is a valid CAS Registry Number.

18319-61-4Downstream Products

18319-61-4Relevant academic research and scientific papers

TRANSFORMATIONS OF TERPENOIDS ON SYNTHETIC ZEOLITES I. REACTIONS OF LABDANE ALCOHOLS ON ZEOLITE HY

Chernenko, G. F.,Kobzar', E. A.,Salakhutdinov, N. F.,Schmidt, E. N.,Bagryanskaya, I. Yu.,Gatilov, Yu. V.

, p. 579 - 587 (1991)

The transformations on zeolite HY of epimanool and of 13-hydroxylabd-8(17),14-dien-6-one and its Δ7,8 isomer have been studied.

CYCLIZATION AND REARRANGEMENT OF DITERPENOIDS. VII. COMPOSITION OF THE HYDROCARBON FRACTION OF A MIXTURE OF THE PRODUCTS OF CYCLIZATION OF MANOOL AND SCLAREOL BY ORDINARY ACIDS

Ungur, N. D.,Barba, A. N.,Vlad, P. F.

, p. 612 - 614 (2007/10/02)

The hydrocarbon fractions of the products of the cyclization of manool and sclareol by a mixture of conc. sulfuric and formic or acetic acids have been investigated.It has been established that they contain, in addition to the Δ8/9-pimaradiene, Δ8(9)-isopimaradiene, roasadiene, and 13-epirosadiene identified previously, the tetracyclic hydrocarbons (1R, 2S, 7S, 11S, 12R, 13R)-2, 6, 6, 11, 13-pentamethyltetracyclo1.10.02.7>pentadeca-9-ene and (1S, 2R, 11S, 12R, 1R)-2, 7, 7, 11, 15-pentamethyltetracyclo2.11.03.8>pentadeca(8)-ene.

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