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The chemical "3β-[3-O-Methyl-4-O-(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl)-2,6-dideoxy-β-D-ribo-hexopyranosyloxy]-14-hydroxy-5β-cardanolide-20(22)-ene" is a complex, naturally occurring glycosylated cardanolide compound. It features a steroidal backbone with a hydroxyl group at the 14th position and a 5β-cardanolide ring structure. The molecule is further characterized by a unique sugar moiety attached at the 3β position, which includes a 2,6-dideoxy-β-D-ribo-hexopyranosyl unit that is 3-O-methylated and 4-O-linked to a disaccharide composed of two β-D-glucopyranosyl units. This intricate structure contributes to the compound's potential biological activities and its role in the plant kingdom, where it may serve various functions such as defense against predators or as a signaling molecule.

9007-56-1

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9007-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 9007-56-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 9,0,0 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 9007-56:
(6*9)+(5*0)+(4*0)+(3*7)+(2*5)+(1*6)=91
91 % 10 = 1
So 9007-56-1 is a valid CAS Registry Number.

9007-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[14-hydroxy-3-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:9007-56-1 SDS

9007-56-1Upstream product

9007-56-1Relevant academic research and scientific papers

Degradation of Cardenolide Glycosides

Kim, Youn Chul,Higuchi, Ryuichi,Komori, Tetsuya,Abe, Fumiko,Yamauchi, Tatsuo

, p. 943 - 947 (2007/10/02)

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.

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