508-04-3 Usage
Chemical Description
α-Amyrin is a triterpene compound found in many plant species.
Description
Α-AMYRIN, a pentacyclic triterpenoid belonging to the oleanane class, is characterized by a double bond between positions 13 and 18 and a hydroxy group at the 3beta position. It is a naturally occurring chemical compound that is widely distributed in nature and can be isolated from various plant sources, such as epicuticular wax.
Uses
Used in Pharmaceutical Industry:
Α-AMYRIN is used as a pharmaceutical compound for its potential therapeutic properties. It has been studied for its anti-inflammatory, anti-cancer, and anti-microbial activities, making it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
In the cosmetic industry, Α-AMYRIN is used as an ingredient in various skincare and beauty products due to its potential benefits for the skin. It may be utilized for its moisturizing, anti-aging, and skin-soothing properties, contributing to the overall effectiveness of these products.
Used in Chemical Research:
Α-AMYRIN is also used in chemical research as a starting material for the synthesis of other bioactive compounds. Its unique structure and properties make it an interesting subject for further investigation and potential applications in various fields.
Used in Traditional Medicine:
Α-AMYRIN has been used in traditional medicine for centuries, particularly in the treatment of various ailments and conditions. Its natural origin and potential health benefits make it a valuable component in the development of alternative and complementary therapies.
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.
508-04-3Relevant 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
