152507-67-0 Usage
General Description
Butyl oleanolate is a chemical compound derived from oleanolic acid, a natural triterpenoid found in various plant sources. It is commonly used in cosmetic and skincare products for its anti-inflammatory, anti-oxidant, and anti-aging properties. Butyl oleanolate has been shown to have skin protective effects, improving skin barrier function and reducing the signs of aging. It is also known for its potential wound healing properties, making it a valuable ingredient in skincare formulations. Additionally, butyl oleanolate has been studied for its potential anti-cancer and anti-viral properties, suggesting a wide range of potential therapeutic uses for this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 152507-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,5,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 152507-67:
(8*1)+(7*5)+(6*2)+(5*5)+(4*0)+(3*7)+(2*6)+(1*7)=120
120 % 10 = 0
So 152507-67-0 is a valid CAS Registry Number.
152507-67-0Relevant articles and documents
Protonated montmorillonite-mediated highly specific isomerization of oleanolic acid esters: Application to the synthesis of Δ13(18)-CDDO-Me
Chen, Dongyin,Zhang, Pu,Sun, Yan,Wang, Pengfei,Zhang, Can,Kong, Lingyi,Zhang, Ji,Sun, Hongbin,Wen, Xiaoan
, p. 11154 - 11161 (2016)
A one-pot highly specific isomerization of oleanolic acid esters (5a-g) to δ-oleanolic acid esters (6a-g) was achieved in the presence of proton-exchanged montmorillonite (H-mont) under mild reaction conditions. This protocol could proceed smoothly on a 15.0 gram scale. Based on this methodology, the synthesis of the biologically active compound Δ13(18)-CDDO-Me (4) was realized.
Mild, one-pot conversion of carboxylic acids into esters using phase transfer catalysis
Puntambekar, Hemalata M,Naik, D G,Kapadi, A H
, p. 793 - 794 (2007/10/02)
One-pot conversion of carboxylic acids into esters under the influence of phase transfer catalysis is reported.The method is shown to work satisfactorily for optically active acids having epimerisable α-hydrogen.
