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508-04-3

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508-04-3 Usage

Chemical Description

α-Amyrin is a triterpene compound found in many plant species.

Uses

α-Amyrin is a natural chemical compound of the triterpene class. It is a pentacyclic triterpenol widely distributed in nature and has been isolated from a variety of plant sources such as epicuticular wax.

Definition

ChEBI: A pentacyclic triterpenoid that is oleanane which has a double bond between positions 13 and 18, and in which the hydrogen at the 3beta position is replaced by a hydroxy group.

Purification Methods

Purify it through an Al2O3 column and eluting with pet ether (40-60o) then Et2O and recrystallising from pet ether or EtOH. The acetate crystallises from Ac2O or pet ether and has m 242-143o and [] D +82.8o (c 0.81, CHCl3) [Crow & Michael Aust J Chem 8 133 1955, Barton et al. J Chem Soc (C) 1031 1968, Beilstein 6 III 1894, 6 IV 4195.]

Check Digit Verification of cas no

The CAS Registry Mumber 508-04-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,0 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 508-04:
(5*5)+(4*0)+(3*8)+(2*0)+(1*4)=53
53 % 10 = 3
So 508-04-3 is a valid CAS Registry Number.

508-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 13(18)-Oleanen-3-ol

1.2 Other means of identification

Product number -
Other names -

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:508-04-3 SDS

508-04-3Upstream product

508-04-3Relevant articles and documents

A short enantioselective total synthesis of the fundamental pentacyclic triterpene lupeol

Surendra, Karavadhi,Corey

supporting information; experimental part, p. 13928 - 13929 (2009/12/25)

(Chemical Equation Presented) The first enantioselective synthesis of lupeol has been developed by applying two carefully crafted cation-π cyclization stages to generate the pentacyclic structure with complete stereocontrol. The synthesis (Scheme 1) is no

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