466-09-1

Basic information

• Product Name: ODORIGENIN B
• Synonyms: 3-beta,14-dihydroxy-5-alpha-card-20(22)-enolide;3-beta-14-beta-5-allo-cardenolid;ODORIGENIN B;UZARIGENIN;3β,14-Dihydroxy-5α-card-20(22)-enolide
• CAS NO: 466-09-1
• Molecular Formula: C23H34O4
• Molecular Weight: 374.51
• EINECS: 207-373-0
• Product Categories: Cardioglycosides & Glycosides
• Mol File: 466-09-1.mol
• Article Data: 12

Chemical Properties

• Melting Point: 240-256°
• Boiling Point: 549.3°Cat760mmHg
• Flash Point: 188.2°C
• Appearance: /
• Density: 1.231g/cm³
• PKA: 14.93±0.70(Predicted)
• CAS DataBase Reference: ODORIGENIN B(CAS DataBase Reference)
• NIST Chemistry Reference: ODORIGENIN B(466-09-1)
• EPA Substance Registry System: ODORIGENIN B(466-09-1)

Safety Data

• Hazardous Substances Data: 466-09-1(Hazardous Substances Data)

Usage

General Description

Odorigenin B is a natural bioactive compound that can be extracted from the flower of Calycanthus chinensis, also known as the Chinese Wax Shrub. It is classified as a phenylpropanoid, a type of aromatic compound that results from the shikimic acid pathway. The structure of odorigenin B consists of a glucose derivative connected to a phenylpropanoid, forming a glycoside. Specific details about the chemical composition, efficacy, and use of odorigenin B are limited. Further research is required to understand its potential biological or therapeutic applications.

Upstream product

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• 6877-82-3 Desglucouzarin 
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• 9007-56-1 odoroside K 
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• 58407-69-5 3β-O-(β-D-diginosyl)-14-hydroxy-5α,14β-card-20(22)-enolide 

Downstream Products

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• 128701-08-6 digitoxigenin palmitate 
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• 514-39-6 3-epiperiplogenin 
• 6877-82-3 3-epidigitoxigenin β-D-glucoside 
• 18531-44-7 periplogenin β-D-glucoside 
• 6877-82-3 digitoxigenin β-D-glucoside 
• 20231-81-6 3-epidigitoxigenin β-D-gentiobioside 
• 35068-75-8 desglucouzarin tetraacetate 
• 2287-95-8 3β,14-dihydroxy-5β,14β-card-20(22)-enolide 3-(3-carboxypropanoate) 

Relevant articles and documents

CARDENOLIDE DIGLYCOSIDES FROM OXYSTELMA ESCULENTUM

Two new cardenolide diglycosides, named oxystelmoside and oxystelmine, were isolated from the dried roots of Oxystelma esculentum.On the basis of chemical and spectroscopic evidence their structures were established as uzarigenin 3-O-β-D-xylopyranosyl(1->4)-O-β-D-digitalopyranoside and periplogenin 3-O-6-deoxy-β-D-glucopyranosyl(1->4)-α-D-digitalopyranoside. Key Word Index - Oxystelma esculentum; Asclepiadaceae; roots; oxystelmoside; oxystelmine; steroid; cardenolide glycoside.

Degradation of Cardenolide Glycosides

The thermal degradation of cardenolide glycosides consisting of different sugar moieties and aglycones was examined.On simple heating, the sugar - aglycone linkage of cardenolide glycosides having 2,6-dideoxy sugar moieties is readily cleaved, to afford their genuine aglycones.On the contrary, cardenolide glycosides possessing 6-deoxy sugar moieties are resistant to the degradative reaction.Besides the fission of the glycosidic linkages, some interesting reactions also took place.The pyrolyzed products were isolated by chromatography, and the structures were elucidated by spectroscopic evidence.

Studies on Cerbera. V. Minor glycosides of 17α-digitoxigenin from the stems of genus Cerbera

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