100462-37-1

Basic information

• Product Name: ROSIRIDIN
• Synonyms: ROSIRIDIN(P);b-D-Glucopyranoside,(2E,4S)-4-hydroxy-3,7-dimethyl-2,6-octadien-1-yl;ROSIRIDIN;(2E,4S)-4-Hydroxy-3,7-dimethyl-2,6-octadien-1-yl beta-D-glucopyranoside;(2E,4S)-4-Hydroxy-3,7-dimethyl-2,6-octadien-1-yl β-D-glucopyranoside, 98%, from Rhodiola rosea L.
• CAS NO: 100462-37-1
• Molecular Formula: C16H28O7
• Molecular Weight: 332.39
• Product Categories: standardized herbal extract;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).
• Mol File: 100462-37-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 563.483 °C at 760 mmHg
• Flash Point: 294.584 °C
• Appearance: /
• Density: 1.26
• Refractive Index: 1.555
• PKA: 12.89±0.70(Predicted)
• CAS DataBase Reference: ROSIRIDIN(CAS DataBase Reference)
• NIST Chemistry Reference: ROSIRIDIN(100462-37-1)
• EPA Substance Registry System: ROSIRIDIN(100462-37-1)

Safety Data

• Hazardous Substances Data: 100462-37-1(Hazardous Substances Data)

Usage

General Description

ROSIRIDIN is a naturally occurring chemical compound found in the plant Rhodiola rosea, which is commonly used in traditional medicine. It is known for its antioxidant and anti-inflammatory properties, and has been studied for its potential therapeutic effects on various health conditions, including stress, fatigue, and depression. ROSIRIDIN has also been shown to have neuroprotective and cardioprotective effects, making it a promising candidate for the development of new pharmaceutical drugs. Additionally, it has been found to have potential benefits for improving cognitive function, enhancing physical performance, and boosting immune system function. Overall, ROSIRIDIN is a versatile compound with a wide range of potential health benefits.

InChI:InChI=1/C16H28O7/c1-9(2)4-5-11(18)10(3)6-7-22-16-15(21)14(20)13(19)12(8-17)23-16/h4,6,11-21H,5,7-8H2,1-3H3/b10-6+/t11-,12-,13-,14+,15-,16-/m1/s1

Upstream product

• 101409-51-2 pentaacetylrosiridin 

Relevant articles and documents

Synthesis and stereochemistry of (-)-rosiridol and (-)-rosiridin

The plant-derived monoterpenoids (-)-rosiridol and (-)-rosiridin can be assembled in an enantioselective manner via DIP-Cl reduction of a ketone precursor obtained by BCl3-mediated C-C coupling of prenyl stannane and an α,β-unsaturated C5 aldehyde. On the basis of Mosher analyses, the absolute stereochemistry 4S was assigned to (-)-rosiridol; this was confirmed by X-ray structure analysis of pentaacetylrosiridin. Glucosylation of (4S)-4-acetoxygeraniol proceeds under Koenigs-Knorr conditions in diethyl ether. (-)-Rosiridin was synthesized for the first time.