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D:A-Friedoolean-3-ene is a naturally occurring triterpene, a type of organic compound derived from plants. It is characterized by a unique carbon skeleton with six fused rings, which gives it a distinct structure. D:A-Friedoolean-3-ene is found in various plant species and is known for its potential biological activities, such as anti-inflammatory and anti-cancer properties. D:A-Friedoolean-3-ene has been the subject of scientific research to understand its role in plant defense mechanisms and its potential applications in medicine and pharmaceuticals. The compound's name reflects its chemical structure, with "D:A" indicating the presence of a double bond, "Friedo" referring to the friedelane core structure, "olean" denoting the oleanane triterpene class, and "-3-ene" specifying the location of the double bond on the third carbon atom.

2735-88-8

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2735-88-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2735-88-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2735-88:
(6*2)+(5*7)+(4*3)+(3*5)+(2*8)+(1*8)=98
98 % 10 = 8
So 2735-88-8 is a valid CAS Registry Number.

2735-88-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name friedel-3(4)-ene

1.2 Other means of identification

Product number -
Other names Friedelen-(3)

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:2735-88-8 SDS

2735-88-8Relevant academic research and scientific papers

Reductive Ring-opening of Triterpenoid Epoxides with Lithium and Ethylenediamine

Sengupta, Pasupati,Das, Kanchan,Das, Saktipada

, p. 1175 - 1177 (2007/10/02)

The reactions of lithium and ethylenediamine with 3α,4α-(I, III) and 3β,4β-epoxides (VIII, IX) of friedel-3-ene afford the hydroxy derivatives via epoxide ring-opening.

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