301-19-9 Usage
Description
Robinin, a flavone belonging to the flavonol glycosides, is found in Robinia species such as Robinia pseudoacacia and in Pueraria and Vigna species. It is known for its antibacterial activity.
Uses
Used in Pharmaceutical Industry:
Robinin is used as an antibacterial agent for its ability to inhibit the growth of certain bacteria, making it a potential candidate for the development of new antibiotics.
Used in Cosmetic Industry:
Due to its antibacterial properties, Robinin can be used in cosmetic products to maintain skin health and prevent infections.
Used in Food Industry:
Robinin can be utilized as a natural preservative in the food industry to prevent bacterial growth and extend the shelf life of products.
Used in Agricultural Industry:
Robinin's antibacterial properties can be applied in agriculture to protect crops from bacterial infections and improve overall yield.
Check Digit Verification of cas no
The CAS Registry Mumber 301-19-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,0 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 301-19:
(5*3)+(4*0)+(3*1)+(2*1)+(1*9)=29
29 % 10 = 9
So 301-19-9 is a valid CAS Registry Number.
InChI:InChI=1/C33H40O19/c1-10-19(36)23(40)26(43)31(47-10)46-9-17-21(38)25(42)28(45)33(51-17)52-30-22(39)18-15(35)7-14(49-32-27(44)24(41)20(37)11(2)48-32)8-16(18)50-29(30)12-3-5-13(34)6-4-12/h3-8,10-11,17,19-21,23-28,31-38,40-45H,9H2,1-2H3/t10-,11-,17+,19-,20-,21-,23+,24+,25-,26+,27+,28+,31+,32-,33-/m0/s1
301-19-9Relevant articles and documents
The final structure of robinin and biorobin and their total synthesis
Farkas,Vermes,Nogradi,Kalman
, p. 215 - 218 (2007/10/10)
Robinin has been proved by total synthesis and by methylation analysis using GC-MS to be kaempferol-3- O-(6-O-α-l-rhamnopyranosyl -β-d-galactopyranoside)-7-O-α-l-rhamnopyranoside and not, as claimed by Maksjutina et al., a mixture of 4 glycosides containing the 7-O-rhamnosyl moiety in the α- and β-furanoside as well as in the α- and β-pyranoside forms. The assumption that the 3-O-rhamnosido -galactose moiety contained furanoid rings was also disproved.