32361-88-9 Usage
Uses
Used in Pharmaceutical Industry:
PANICULATIN is used as a pharmaceutical agent for its potential therapeutic properties. The hydroxy and glycosidic groups present in its structure allow it to interact with biopolymers and macromolecules, making it a promising candidate for the development of new drugs and treatments.
Used in Cosmetic Industry:
In the cosmetic industry, PANICULATIN is used as an active ingredient for its potential skin benefits. The hydroxy groups and glycosidic linkages in its structure may contribute to its antioxidant, anti-inflammatory, and skin-soothing properties, making it suitable for inclusion in skincare products.
Used in Food Industry:
PANICULATIN can be used as a natural food additive for its potential health benefits. The presence of hydroxy and glycosidic groups may provide antioxidant and anti-inflammatory effects, which can be beneficial in enhancing the nutritional value and health-promoting properties of food products.
Check Digit Verification of cas no
The CAS Registry Mumber 32361-88-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32361-88:
(7*3)+(6*2)+(5*3)+(4*6)+(3*1)+(2*8)+(1*8)=99
99 % 10 = 9
So 32361-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C27H30O15/c28-5-11-17(32)21(36)23(38)26(41-11)14-19(34)13-16(31)10(8-1-3-9(30)4-2-8)7-40-25(13)15(20(14)35)27-24(39)22(37)18(33)12(6-29)42-27/h1-4,7,11-12,17-18,21-24,26-30,32-39H,5-6H2/t11-,12-,17-,18-,21+,22+,23-,24-,26+,27+/m1/s1
32361-88-9Relevant academic research and scientific papers
Total synthesis of two isoflavone bis-C-glycosides: Genistein and orobol 6,8-Di-C-β-D-glucopyranosides
Sato, Shingo,Ishikawa, Hidetoshi
experimental part, p. 3126 - 3130 (2010/11/04)
This paper describes the first successful synthesis of two isoflavone bis-C-glycosides, genistein and orobol 6,8-di-C-β-D-glucopyranosides from phloroacetophenone bis-C-glycoside in total yields of 27 and 19%, respectively, using a four-step reaction: dir
