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50906-66-6

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  • b-D-Glucopyranoside,1,4a,5,6,7,7a-hexahydro-5,7-dihydroxy-7-methylcyclopenta[c]pyran-1-yl

    Cas No: 50906-66-6

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50906-66-6 Usage

Cyclopentane ring structure

The compound has a five-membered ring structure with alternating single and double bonds.

Hydroxyl groups

The compound contains two hydroxyl (-OH) groups attached to the cyclopentane ring, which can form hydrogen bonds and interact with other molecules.

Methyl group

A methyl (-CH3) group is attached to the cyclopentane ring, providing steric hindrance and affecting the compound's reactivity and polarity.

Hexahydro

The compound has six hydrogen atoms added to the cyclopentane ring, which may contribute to its stability and solubility.

Dihydroxy

The compound has two hydroxyl groups, which can participate in hydrogen bonding and other interactions.

Glucopyranoside group

The compound contains a beta-D-glucopyranoside group, which is a sugar molecule derived from glucose. This suggests that the compound may have biological activity or be involved in metabolic processes.

Natural product

The compound is likely derived from plants or microorganisms, given its complex structure and the presence of a sugar moiety.

Potential pharmaceutical or medicinal applications

The presence of hydroxyl groups and the unique structure of the compound suggest that it may have potential pharmaceutical or medicinal applications, although further research is needed to confirm this.

Biological activity

The compound's hydroxyl groups and complex structure may allow it to interact with biological systems, potentially leading to biological activity.

Further research needed

More research is required to fully understand the properties, potential uses, and mechanisms of action of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 50906-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,9,0 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50906-66:
(7*5)+(6*0)+(5*9)+(4*0)+(3*6)+(2*6)+(1*6)=116
116 % 10 = 6
So 50906-66-6 is a valid CAS Registry Number.

50906-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R,4S,5S,6R)-2-[(5,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

1.2 Other means of identification

Product number -
Other names Leonuridine

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:50906-66-6 SDS

50906-66-6Upstream product

50906-66-6Downstream Products

50906-66-6Relevant articles and documents

A new polyoxygenated triterpene and two new aeginetic acid quinovosides from the roots of Rehmannia glutinosa

Lee, So Young,Kim, Ju Sun,Choi, Ran Joo,Kim, Yeong Shik,Lee, Je-Hyun,Kang, Sam Sik

experimental part, p. 742 - 746 (2011/07/08)

A new minor polyoxygenated triterpene named glutinolic acid (1) and two new aeginetic acid quinovosides (2, 3) were isolated from the roots of Rehmannia glutinosa LIBOSCH. (Scrophulariaceae) cultivated in Gunwi-gun, Korea. The structures of these compounds were established as 3 α,19 α,20 β,24,30-pentahydroxyurs-12-en-28-oic acid (1, glutinolic acid), aeginetic acid 5-O- β-D-quinovoside (2) and aeginetoyl ajugol 5″-O- β-D-quinovoside (3) on the basis of chemical and spectroscopic evidence.

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