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466-09-1

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466-09-1 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.

Check Digit Verification of cas no

The CAS Registry Mumber 466-09-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 466-09:
(5*4)+(4*6)+(3*6)+(2*0)+(1*9)=71
71 % 10 = 1
So 466-09-1 is a valid CAS Registry Number.

466-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β,14-dihydroxy-5α,14β-card-20(22)-enolide

1.2 Other means of identification

Product number -
Other names UZARIGENIN

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:466-09-1 SDS

466-09-1Relevant articles and documents

CARDENOLIDE DIGLYCOSIDES FROM OXYSTELMA ESCULENTUM

Srivastava, Suman,Khare, Maheshwari P.,Khare, Anakshi

, p. 1019 - 1022 (2007/10/02)

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.

BIOTRANSFORMATION OF DIGITOXIGENIN BY GINSENG HAIRY ROOT CULTURES

Kawaguchi, Kiichiro,Hirotani, Masao,Yoshikawa, Takafumi,Furuya, Tsutomu

, p. 837 - 843 (2007/10/02)

Five new compounds (three esters and two glycosides) and seven previously reported compounds were isolated as biotransformation products of digitoxigenin by ginseng hairy root cultures.The new esters and glycosides were elucidated as digitoxigenin stearate, digitoxigenin palmitate, digitoxigenin myristate, 3-epidigitoxigenin β-D-gentiobioside and digitoxigenin β-D-sophoroside using 1H and 13C NMR and FAB mass spectral data.Biotransformations involving esterification (of stearic acid, palmitic acid, myristic acid and lauric acid) and glycosylation (of gentiobiose and sophorose) of digitoxigenin have been demonstrated for the first time in the plant cell and tissue cultures.The hairy roots showed high glycosylation ability to the digitoxigenin molecule.

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

Yamauchi,Abe,Wan

, p. 4993 - 4995,4993-4995 (2007/10/02)

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