136172-60-6 Usage
General Description
6-O-Caffeoylarbutin is a chemical compound found in plants that belongs to the class of hydroxycinnamic acid derivatives. It is derived from caffeic acid and arbutin, and it possesses antioxidant and anti-inflammatory properties. 6-O-Caffeoylarbutin is commonly found in various medicinal plants, such as Paeonia lactiflora, and has been studied for its potential health benefits. Some research suggests that this compound may have anti-aging effects by protecting against oxidative stress and reducing inflammation. Additionally, it has been found to inhibit the production of melanin, indicating potential use in skin-lightening products. However, further studies are needed to fully understand the biological activities and potential applications of 6-O-Caffeoylarbutin.
Check Digit Verification of cas no
The CAS Registry Mumber 136172-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,7 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 136172-60:
(8*1)+(7*3)+(6*6)+(5*1)+(4*7)+(3*2)+(2*6)+(1*0)=116
116 % 10 = 6
So 136172-60-6 is a valid CAS Registry Number.
136172-60-6Relevant articles and documents
A highly efficient transformation of cis- to trans-cinnamic acid derivatives by iodine
Li, Zhen-Jie,Cai, Le,Mei, Rui-Feng,Dong, Jian-Wei,Li, Shu-Quan,Yang, Xue-Qiong,Zhou, Hao,Yin, Tian-Peng,Ding, Zhong-Tao
supporting information, p. 7197 - 7200 (2015/12/12)
Cinnamic acid derivatives (CAs), which have proven to be versatile components, are present in abundance in biologically active natural products, and are widely used as intermediates in the manufacture of pharmaceuticals, and chemicals. The presence of cis- and trans-CAs created difficulties for natural product and organic synthetic studies. A highly efficient method that utilized iodine to entirely convert cis- CAs into their trans-forms was developed to solve this problem. The mechanism of study revealed this conversion occurred via an anti-diiodo intermediate.
