2545-00-8 Usage
Description
AFZELECHIN, also known as a tetrahydroxyflavan, is a flavan compound characterized by its (2S)-flavan structure substituted with hydroxy groups at positions 3, 5, 7, and 4'. This unique structure endows AFZELECHIN with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
AFZELECHIN is used as a pharmaceutical compound for its potential therapeutic properties. Its hydroxy-substituted structure allows for interactions with various biological targets, making it a candidate for the development of new drugs.
Used in Cosmetic Industry:
AFZELECHIN is used as an active ingredient in cosmetics for its antioxidant and skin-protective properties. Its ability to scavenge free radicals and protect the skin from environmental stressors makes it a valuable component in skincare products.
Used in Food Industry:
AFZELECHIN is used as a natural food additive for its antioxidant and preservative properties. Its ability to extend the shelf life of food products and maintain their quality makes it a beneficial component in the food industry.
Used in Nutraceutical Industry:
AFZELECHIN is used as a nutraceutical ingredient for its potential health benefits. Its antioxidant and anti-inflammatory properties make it a promising candidate for the development of dietary supplements and functional foods.
Check Digit Verification of cas no
The CAS Registry Mumber 2545-00-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2545-00:
(6*2)+(5*5)+(4*4)+(3*5)+(2*0)+(1*0)=68
68 % 10 = 8
So 2545-00-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O5/c16-9-3-1-8(2-4-9)15-13(19)7-11-12(18)5-10(17)6-14(11)20-15/h1-6,13,15-19H,7H2
2545-00-8Relevant articles and documents
General synthesis of epi-series catechins and their 3-gallates: Reverse polarity strategy
Ohmori, Ken,Yano, Takahisa,Suzuki, Keisuke
supporting information; experimental part, p. 2693 - 2696 (2010/08/21)
A general synthetic route to the epi-series catechins was developed based on the reverse polarity strategy. Aromatic nucleophilic substitution reaction followed by the sulfinyl-metal exchange and cyclization enabled stereo-controlled access to various members of epi-series catechins and their 3-gallates.
New oligomeric proanthocyanidine from Ziziphus jujuba
Malik, Aibek,Kuliev,Akhmedov,Vdovin,Abdullaev
, p. 40 - 42 (2007/10/03)
Chemical and spectral data establish the structure of an oligomeric proanthocyanidine PZ-5 isolated from Ziziphus jujuba.
(+)-AFZELECHIN 3-RHAMNOSIDE FROM CASSIPOUREA GERRARDII
Drewes, Siegfried E.,Taylor, Craig W.,Cunningham, Anthony B.
, p. 1073 - 1075 (2007/10/02)
A new flavanol glycoside has been isolated from the bark of Cassipourea gerrardii.Its structure has been established from spectroscopic and hydrolytic studies as (+)-afzelechin 3-O-α-L-rhamnopyranoside.Delayed homonuclear COSY studies show up interesting long-range couplings between specific protons. Key words: Cassipourea gerrardii; Rhizophoraceae; bark; (+)-afzelechin 3-O-α-L-rhamnopyranoside.
