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(20S)-3β,16α,28-Trihydroxyolean-12-en-29-al is a naturally occurring triterpenoid compound characterized by its unique molecular structure. This chemical is derived from the oleanane family of triterpenoids, which are known for their diverse range of biological activities, including anti-inflammatory, anti-cancer, and anti-viral properties. The specific stereochemistry of the compound, with hydroxyl groups at the 3β, 16α, and 28 positions, and an aldehyde group at the 29 position, contributes to its distinct biological profile. Research on such compounds is important for understanding their potential therapeutic applications and for the development of new drugs based on their chemical structures.

5172-35-0

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5172-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5172-35-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5172-35:
(6*5)+(5*1)+(4*7)+(3*2)+(2*3)+(1*5)=80
80 % 10 = 0
So 5172-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O4/c1-25(2)21-9-12-28(5)22(27(21,4)11-10-23(25)33)8-7-19-20-15-26(3,17-31)13-14-30(20,18-32)24(34)16-29(19,28)6/h7,17,20-24,32-34H,8-16,18H2,1-6H3/t20-,21-,22+,23-,24+,26-,27-,28+,29+,30+/m0/s1

5172-35-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,4aS,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5,10-dihydroxy-4a-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names Olean-12-en-29-al,3,16,28-trihydroxy-,(3beta,16alpha,20beta)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5172-35-0 SDS

5172-35-0Relevant academic research and scientific papers

SAPONINS IN CYCLAMEN SPECIES: CONFIGURATION OF CYCLAMIRETIN C AND STRUCTURE OF ISOCYCLAMIN

Reznicek, Gottfried,Jurenitsch, Johann,Robien, Wolfgang,Kubelka, Wolfgang

, p. 825 - 828 (2007/10/02)

Five sapogenins and three saponins were identified in bulbs of 14 cytologically defined Cyclamen species and their structures were determined by means of mass, 1H and 13C NMR spectroscopy.In addition to the known products of hydrolysis, primulagenin A was found, and cyclamiretin C was shown to be identical with cyclamigenin C.The new saponin isocyclamin was identified as 3β--O-β-D-glucopyranosyl-(1-4)--α-L-arabinopyranosyl>-16α-hydroxy-13β,28-epoxy-olean-30-al. - Key Word Index - Cyclamen; Primulaceae; saponin; sapogenin; chemotaxonomy.

SAPONINS FROM PRIMULA DENTICULATA

Ahmad, Viqar Uddin,Sultana, Viqar,Arif, Shoib,Saqib, Qazi Najmus

, p. 304 - 306 (2007/10/02)

A new triterpenoid saponin, primulanin, isolated from the whole plant of Primula denticulata was characterized as 3-O2)-β-D-glucopyranosyl-(1->4)-α-L-arabinopyranosyloxy>-16α-hydroxy-13β,28-epoxy-olean-30-al.Key Word Index - Primula denticulata; Primulaceae; triterpenoid saponins; primulanin; saxifragifolin B.

Structure Elucidation of Two Triterpenoid Tetrasaccharides from Androsace saxifragifolia

Waltho, Jonathan P.,Williams, Dudley H.,Mahato, Shashi B.,Pal, Bikas C.,Barna, Jennifer C. J.

, p. 1527 - 1532 (2007/10/02)

Saxifragifolins A and B, two new triterpenoid tetrasaccharides isolated from the aerial part of Androsace saxifragifolia, were respectively shown to be androsacenol-3-O-2)-β-D-glucopyranosyl-(1-->4)-(β-D-glucopyranosyl-(1-->2))-α-L-arabinopyranoside> (1) and cyclamiretin A 3-O-2)-β-D-glucopyranosyl-(1-->4)-(β-D-glucopyranosyl-(1-->2))-α-L-arabinopyranoside> (2).The structural details were elucidated by a combination of fast atom-bombardment mass spectrometry, chemical degradation, and one- and two-dimensional n.m.r. spectroscopy.

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