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"2β,4aα,8α-Trihydroxy-1β,8β-dimethylgibbane-1α,10β-dicarboxylic acid 1,4a-lactone" is a complex organic compound with a unique molecular structure. It is characterized by the presence of three hydroxyl groups at the 2β, 4aα, and 8α positions, a dimethyl group at the 1β and 8β positions, and two carboxylic acid groups at the 1α and 10β positions. The compound also features a lactone ring formed between the 1 and 4a positions, which contributes to its stability and reactivity. This molecule is of interest in the field of organic chemistry, particularly in the study of natural products and their derivatives, due to its intricate structure and potential applications in pharmaceuticals or other chemical industries.

561-68-2

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561-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 561-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 561-68:
(5*5)+(4*6)+(3*1)+(2*6)+(1*8)=72
72 % 10 = 2
So 561-68-2 is a valid CAS Registry Number.

561-68-2Downstream Products

561-68-2Relevant academic research and scientific papers

THE STEREOCHEMISTRY OF SOME REACTIONS AT C-16 IN GIBBERELLINS; AN X-RAY CRYSTALLOGRAPHIC STUDY OF THE METHYL ESTERS OF GIBBERELLIN A2 AND GIBBERRLLIN A2 HYDROCHLORIDE

Abouamer, Karima M.,Hanson, James R.,Hitchcock, Peter B.

, p. 1991 - 1994 (2007/10/02)

Hydration of the 16-ene in the gibberillins is shown, by a combination of spectroscopic and X-ray crystallographic means, to lead to (16R)-alcohols.The hydrochloride of gibberellin A9 methyl ester possesses the same (16R)-stereochemistry.

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