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Alloyohimbone is a naturally occurring chemical compound found in the bark of the Pausinystalia yohimbe tree, native to Central and Western Africa. It is an indole alkaloid, similar to yohimbine, and is known for its potential aphrodisiac and stimulant properties. Alloyohimbone has been traditionally used in folk medicine for its alleged benefits in treating erectile dysfunction, anxiety, and depression. However, scientific research on its efficacy and safety is limited, and it is not approved by regulatory agencies like the FDA for any medical use. It is important to note that the use of alloyohimbone, like other unregulated substances, may carry potential risks and side effects, and its consumption should be approached with caution.

483-29-4

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483-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 483-29-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 483-29:
(5*4)+(4*8)+(3*3)+(2*2)+(1*9)=74
74 % 10 = 4
So 483-29-4 is a valid CAS Registry Number.

483-29-4Downstream Products

483-29-4Relevant academic research and scientific papers

A New ABCDE> Cycloaddition Strategy for the Approach to Yohimbe Alkaloids: Stereoselective Synthesis of (+/-)-3-epi-allo-Yohimbone

Gomez-Pardo, Domingo,d'Angelo, Jean

, p. 6637 - 6640 (2007/10/02)

Diels-Alder cycloaddition between lactam-sulfone 9 and diene 10 led to adducts 11 + 12 (30:1, respectively).Compound 11 has been converted in 4 steps into (+/-)-3-epi-allo-yohimbone 16.Key words: Diels-Alder cycloaddition, Yohimbe alkaloids, (+/-)-3-epi-a

GENERAL METHODS OF SYNTHESIS OF INDOLE ALKALOIDS - 14. SHORT ROUTES OF CONSTRUCTION OF YOHIMBOID AND AJMALICINOID ALKALOID SYSTEMS AND THEIR 13C NUCLEAR MAGNETIC RESONANCE SPECTRAL ANALYSIS.

Wenkert,Chang,Chawla,Cochran,Hagaman,King,orito

, p. 3645 - 3661 (2007/10/04)

Conceptually new schemes of synthesis of indole alkaloids are introduced. The yohimboid ring system is constructed by the sequential treatment of 1-tryptophyl-3-( beta -ketobutyl)pyridinium bromide with base and acid. Hydrogenation of the product yields d,l-pseudoyohimbone. The ajmalicinoid ring system is formed by the exposure of 1-tryptophyl-3-acetylpyridinium bromide to sodio dimethyl malonate and then to acid, followed by hydrogenation. Subsequent reduction and dehydration of the products lead to the racemates of the alkaloids tetrahydroalstonine and akuammigine as well as isomers of ajmalicine. Shifts of specific carbons are found to be of stereochemically diagnostic value.

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