17015-60-0 Usage
Description
Bakuchiol is a natural chemical compound derived from the seeds and leaves of the Psoralea corylifolia plant. It has gained attention in the skincare industry for its potential anti-aging and skin-brightening properties. Often referred to as a natural alternative to retinol, bakuchiol has been found to have similar effects on the skin, such as stimulating collagen production and reducing the appearance of wrinkles and fine lines. Its anti-inflammatory and antioxidant properties also make it a popular ingredient in skincare products, where it is used to help improve the overall health and appearance of the skin while being gentle and well-tolerated, especially by those with sensitive skin.
Uses
Used in Skincare Industry:
Bakuchiol is used as an anti-aging agent for its ability to stimulate collagen production and reduce the appearance of wrinkles and fine lines.
Bakuchiol is used as a skin-brightening agent for its potential to reduce hyperpigmentation and improve overall skin tone.
Bakuchiol is used as an anti-inflammatory agent for its ability to soothe and calm the skin, making it suitable for those with sensitive skin.
Bakuchiol is used as an antioxidant agent for its potential to protect the skin from environmental stressors and promote overall skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 17015-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,1 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17015-60:
(7*1)+(6*7)+(5*0)+(4*1)+(3*5)+(2*6)+(1*0)=80
80 % 10 = 0
So 17015-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H24O/c1-5-18(4,13-6-7-15(2)3)14-12-16-8-10-17(19)11-9-16/h5,7-12,14,19H,1,6,13H2,2-4H3/b14-12+/t18-/m1/s1
17015-60-0Relevant articles and documents
Enantioselective Synthesis of Quaternary Stereocenters via Chromium Catalysis
Xiong, Yang,Zhang, Guozhu
supporting information, p. 5094 - 5097 (2016/10/14)
Asymmetric allylation of aldehydes with γ-disubstituted allyl halides has been achieved in the presence of a sulfonamide/oxazoline chromium complex. A variety of synthetically useful α-homoallylic alcohols with two consecutive stereogenic centers, including one quaternary carbon, can be accessed in a highly diastereoselective and enantioselective manner.
A short synthesis of (+)-bakuchiol
Esumi, Tomoyuki,Yamamoto, Chihiro,Fukuyama, Yoshiyasu
, p. 1845 - 1847 (2013/09/12)
The concise enantioselective total synthesis of (+)-bakuchiol has been achieved using an asymmetric 1,4-addition to construct its all-carbon chiral quaternary center based on the induction of chirality by the (2′S)-2′-phenyloxazolidinone auxiliary, followed by a one-pot transformation under aldol reaction conditions. The synthesis was completed in four steps from (E)-geranic acid in an overall yield of 53%. Georg Thieme Verlag Stuttgart · New York.
Asymmetric construction of all-carbon quaternary stereocenters by chiral-auxiliary-mediated claisen rearrangement and total synthesis of (+)-Bakuchiol
Takao, Ken-Ichi,Shu, Sakamoto,Touati, Marianne Ayaka,Kusakawa, Yusuke,Tadano, Kin-Ichi
, p. 13330 - 13344 (2013/02/23)
An asymmetric Claisen rearrangement using Oppolzer's camphorsultam was developed. Under thermal conditions, a geraniol-derived substrate underwent the rearrangement with good stereoselectivity. The absolute configuration of the newly formed all-carbon quaternary stereocenter was confirmed by the total synthesis of (+)-bakuchiol from the rearrangement product.