139906-05-1 Usage
Class
Flavonoids
Type
Natural polyphenolic compound
Occurrence
Found in various fruits, nuts, and seeds
Antioxidant
Helps protect cells from damage caused by free radicals
Anti-inflammatory
May reduce inflammation in the body
Anti-cancer
Potentially inhibits cancer cell growth
Anti-diabetic
May help regulate blood sugar levels
Cardiovascular health
Supports heart health and improves blood circulation
Interest
Significant interest in the field of natural medicine and nutrition due to its potential therapeutic effects
Structure
The compound has a complex structure with multiple hydroxyl groups, sugar moieties, and a benzopyrylium core
Functional groups
Contains phenolic hydroxyl groups, alkenyl groups, and sugar moieties (beta-D-glucopyranosyl and beta-D-xylopyranosyl)
Solubility
Likely soluble in water due to the presence of hydroxyl and sugar groups, but the exact solubility is not provided in the material
Stability
The stability of procyanidin B1 is not explicitly mentioned in the material, but flavonoids are generally sensitive to light, heat, and pH changes
Applications
Used in the study of natural medicine and nutrition for its potential health benefits, including antioxidant, anti-inflammatory, anti-cancer, and anti-diabetic properties, as well as its cardiovascular health benefits
Check Digit Verification of cas no
The CAS Registry Mumber 139906-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,9,0 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139906-05:
(8*1)+(7*3)+(6*9)+(5*9)+(4*0)+(3*6)+(2*0)+(1*5)=151
151 % 10 = 1
So 139906-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C41H44O22.ClH/c42-13-27-31(50)33(52)36(55)40(61-27)59-25-11-19(44)10-24-20(25)12-26(37(58-24)17-4-7-21(45)22(46)9-17)60-41-38(63-39-35(54)30(49)23(47)14-57-39)34(53)32(51)28(62-41)15-56-29(48)8-3-16-1-5-18(43)6-2-16;/h1-12,23,27-28,30-36,38-42,47,49-55H,13-15H2,(H3-,43,44,45,46,48);1H/t23-,27-,28-,30+,31-,32-,33+,34+,35-,36-,38-,39+,40-,41-;/m1./s1