107915-41-3

Basic information

• Product Name: Flavone, 6-amino-3-hydroxy- (6CI)
• Synonyms: Flavone, 6-amino-3-hydroxy- (6CI)
• CAS NO: 107915-41-3
• Molecular Formula: C₁₅H₁₁NO₃
• Molecular Weight: 253.25274
• Product Categories: FLAVONE
• Mol File: 107915-41-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Flavone, 6-amino-3-hydroxy- (6CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Flavone, 6-amino-3-hydroxy- (6CI)(107915-41-3)
• EPA Substance Registry System: Flavone, 6-amino-3-hydroxy- (6CI)(107915-41-3)

Safety Data

• Hazardous Substances Data: 107915-41-3(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 24449-58-9 5′-acetamino-2′-hydroxychalcone 
• 7298-67-1 5-acetamido-2-hydroxyacetophenone 
• 109093-42-7 N-(3-hydroxy-4-oxo-2-phenyl-4H-chromen-6-yl)acetamide 

Downstream Products

• 1085488-90-9 6-(hydroxycarbonylethylcarbonylamino)flavonol 

Relevant articles and documents

Flavonols

A compound of the formula (I): wherein R is selected from the group consisting of H, alkyl, alkenyl, alkynyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl and acyl, each of which may be optionally substituted;R1 is an organic moiety that is capable of being converted into a charged group;each X and Y is independently selected from the group consisting of H, halogen, —CN, —NO2, —CF3, —OCF3, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, heteroalkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, arylalkenyl, cycloalkylheteroalkyl, arylheteroalkyl, heterocycloalkylheteroalkyl, heteroarylheteroalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl, alkenyloxy, alkynyloxy, cycloalkyloxy, heterocycloalkyloxy, aryloxy, heteroaryloxy, arylalkyloxy, phenoxy, benzyloxy, amino, alkylamino, aminoalkyl, acylamino, arylamino, sulfonylamino, sulfinylamino, —COOH, —COR2, —COOR2, —CONHR2, —NHCOR2, —NHCOOR2, —NHCONHR2, C(═NOH)R2, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, SR2 and acyl, each of which may be optionally substituted;each R2 is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, haloalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, and acyl, each of which may be optionally substituted;m is an integer selected from the group consisting of 0, 1, 2, 3, 4 and 5;p is an integer selected from 0, 1, 2 and 3; or a pharmaceutically acceptable salt or prodrug thereof.

Anti-HIV and antiplasmodial activity of original flavonoid derivatives

In our search for potent anti-HIV and antiplasmodial agents, novel series of flavonoid derivatives and their chalcone intermediates were synthesized and evaluated for inhibition of HIV multiplication and antiproliferative activity on Plasmodium falciparum