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83644-00-2

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83644-00-2 Usage

General Description

Rooperol is a chemical compound belonging to the class of rotenoids, which are natural products with various biological activities. It is isolated from the roots of the plant Boerhavia diffusa, commonly known as punarnava. Rooperol has been found to exhibit anti-inflammatory, antioxidant, and anti-cancer properties in various studies. It has also been investigated for its ability to inhibit the growth and metastasis of cancer cells. Additionally, rooperol has shown potential as a neuroprotective agent and may have applications in the treatment of neurodegenerative diseases.Overall, rooperol is an interesting compound with diverse biological activities and has the potential for further development in the fields of medicine and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 83644-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,4 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83644-00:
(7*8)+(6*3)+(5*6)+(4*4)+(3*4)+(2*0)+(1*0)=132
132 % 10 = 2
So 83644-00-2 is a valid CAS Registry Number.

83644-00-2SDS

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 4-[(E)-5-(3,4-dihydroxyphenyl)pent-1-en-4-ynyl]benzene-1,2-diol

1.2 Other means of identification

Product number -
Other names P2-Bdhpp

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:83644-00-2 SDS

83644-00-2Relevant articles and documents

A concise synthesis of rooperol and related 1,5-diarylpent-1-en-4-ynes

Kerwin, Sean M.,Cha, Jonathan

supporting information, p. 137 - 141 (2014/01/06)

Two powerful strategies: rapid construction of allylic alkynoates via cyclopropenium ion chemistry and mild, palladium-catalyzed decarboxylative coupling were employed in a concise, 5-steps synthesis of the natural product rooperol. The overall approach a

Research on African medicinal plants. II. Hypoxoside, a new glycoside of uncommon structure from Hypoxis obtusa Busch

Marini Bettolo,Patamia,Nicoletti,et al.

, p. 1683 - 1687 (2007/10/02)

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