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5α-Cycloartan-3-one is a naturally occurring triterpenoid compound, characterized by its unique chemical structure featuring a cyclopentane ring fused to a cyclohexane ring, with a ketone functional group at the C-3 position. This organic molecule is derived from the cycloartane family of steroids, which are known for their diverse biological activities. 5α-Cycloartan-3-one has been found in various plant species and has been studied for its potential pharmacological properties, including anti-inflammatory and cytotoxic effects. Its chemical formula is C30H50O, and it is a white crystalline solid with a molecular weight of approximately 426.72 g/mol. The compound's structure and biological activities make it a subject of interest in the field of natural product chemistry and drug discovery.

4936-10-1

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4936-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4936-10-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4936-10:
(6*4)+(5*9)+(4*3)+(3*6)+(2*1)+(1*0)=101
101 % 10 = 1
So 4936-10-1 is a valid CAS Registry Number.

4936-10-1Relevant academic research and scientific papers

CYCLOARTANES AND OTHER TERPENOIDS AND PHENYLPROPANOIDS FROM MONOCYCLANTHUS VIGNEI

Achenbach, Hans,Frey, Dieter

, p. 4263 - 4274 (1992)

From the petrol extract of the stem bark of Monocyclanthus vignei 30 terpenoids and two phenylpropanoids have been isolated and their structures established, among them 17 new cycloartane-type compounds.Geranic acid and β-caryophyllene were found to be the major constituents. Key words: Monocyclanthus vignei; Annonaceae; stem bark; cycloartanes; sterols; sesquiterpenes; geranic acid; phenylpropanoids.

BUXUS ALKALOIDS. PART XI. THE SYNTHESIS OF CYCLOPROTOBUXINE-A (3β,20S-CHIRALITY) AND ITS TWO ISOMERIC ALKALOIDS WITH 3β,20R- AND 3α,20R- CONFIGURATION FROM LANOSTEROL.

Nakano, Tatsuhiko,Martin, Alfonso,Alonso, Miguel

, p. 2957 - 2968 (2007/10/02)

The synthesis of cycloprotobuxine-A (5), representative of Buxus alkaloids, and its two isomeric alkaloids with 3β,20R- and 3α,20R-configuration, from lanosterol, is described.In order to confirm the stereochemistries at C-3 and C-20 in these three alkaloids, the 3β-dimethylamino-(27) and the 3α-dimethylamino derivative (28) of cycloartanol (24) were also synthesised and their 1H and 13C n.m.r.spectra are discussed.

FERN CONSTITUENTS: TRITERPENOIDS ISOLATED FROM POLYPODIUM VULGARE, P. FAURIEI AND P. VIRGINIANUM

Arai, Yoko,Yamaide, Motoko,Yamazaki, Sachiko,Ageta, Hiroyuki

, p. 3369 - 3377 (2007/10/02)

Key Word Index - Polypodium vulgare; P. fauriei; P. virginianum; Polypodiaceae; rhizomes; hop-22(29)-ene; isohop-22(29)-ene; fernenes; serrat-14-ene; dammaradienes; eupha-7,21-diene; cycloartanoid; cyclopodmenyl acetate.The fresh rhizomes of Polypodium vulgare, P. fauriei and P. virginianum collected in Japan gave, in addition to 30 known compounds, three new triterpenoids; dammara-17,21-diene, cyclopodmenyl acetate and 21αH-hopan-22-ol, The structures were elucidated by their physical data and chemical correlations.

New Triterpenes from Swietenia mahagoni Linn: Part V - Scission of C10-C19 Bond of Cyclopropane Ring in Cycloartenol

Narayana, V. Lakshmi,Murthy, Y. L. N.,Row, L. R.

, p. 977 - 978 (2007/10/02)

A successful method is described for the first time to open the cyclopropane ring of cycloartenol (III) to yield 9β-hydroxymethyl derivative (X), in an attempt to establish the biogenetic origin of 9β-hydroxymethyl in cucurbitacins (I).Cycloartanone (VI) is first converted into cycl-1-en-3-one (IV), which rearranges in presence of ethanol-sulphuric acid to yield 9β-hydroxymethyllanosta-1(10)-en-3-one (X).

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