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[(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside is a complex organic compound derived from the roots of the Rehmannia glutinosa herb. It is characterized by its unique molecular structure, which includes multiple hydroxy and methyl groups, as well as a cyclohexane ring and a glucose moiety. [(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside exhibits potential biological activities and has been the subject of research for its potential applications in various fields.

104112-06-3

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104112-06-3 Usage

Uses

Used in Pharmaceutical Applications:
[(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside is used as a pharmaceutical agent for its potential anti-asthmatic properties. The compound may help in the treatment of asthma by modulating the immune response and reducing inflammation in the airways.
Used in Drug Delivery Systems:
In the field of drug delivery, [(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside can be employed as a carrier molecule to improve the bioavailability and targeting of therapeutic agents. Its unique structure and functional groups may allow for the development of novel drug delivery systems, enhancing the efficacy and safety of various medications.
Used in Cosmetics Industry:
[(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside may also find applications in the cosmetics industry due to its potential skin-friendly properties. It could be used as an ingredient in skincare products, potentially offering moisturizing, anti-inflammatory, or antioxidant benefits.
Used in Research and Development:
Due to its complex structure and potential biological activities, [(1R)-1α,3,3-Trimethyl-2α-hydroxy-2-[(1E,3S)-3-hydroxy-1-butenyl]cyclohexan-1β-yl]β-D-glucopyranoside is a valuable compound for research and development in the fields of chemistry, biology, and pharmacology. It can be used as a starting material for the synthesis of new compounds or as a model for studying the interactions between molecules and biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 104112-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,1 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104112-06:
(8*1)+(7*0)+(6*4)+(5*1)+(4*1)+(3*2)+(2*0)+(1*6)=53
53 % 10 = 3
So 104112-06-3 is a valid CAS Registry Number.

104112-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name rehmaionoside A

1.2 Other means of identification

Product number -
Other names (2S,3R,4S,5S,6R)-2-[(1R,2R)-2-Hydroxy-2-((E)-(S)-3-hydroxy-but-1-enyl)-1,3,3-trimethyl-cyclohexyloxy]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol

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:104112-06-3 SDS

104112-06-3Relevant academic research and scientific papers

Chemical studies on crude drug processing. IX. On the constituents of rehmanniae radix. (3). Absolute stereostructures of rehmaionosides A, B, and C, and rehmapicroside, biologically active ionone glucosides and a monoterpene glucoside isolated from Chine

Yoshikawa,Fukuda,Taniyama,Kitagawa

, p. 41 - 47 (2007/10/03)

Following the characterization of the iridoid and iridoid glycoside constituents in Chinese Rehmanniae Radix, the dried root of Rehmannia glutinosa LIBOSCH. [Kan-jio in Japanese], we investigated the structures of biologically active ionone glucosides, re

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