215999-39-6 Usage
Description
3-bromo-6-methoxy-2-phenyl-4H-chromen-4-one, also known as 6-Methoxy-3-bromo-2-phenyl-4H-chromen-4-one, is a heterocyclic chemical compound belonging to the class of chromenones. It features a chromenone ring structure, which is a significant pharmacophore in medicinal chemistry. Identified by its bromine and methoxy functional groups, as well as a phenyl substituent, this compound has demonstrated potential biological activities, particularly in antitumor and antiproliferative properties. Its study and potential applications are primarily focused on drug development and research related to its pharmacological activities.
Uses
Used in Pharmaceutical Industry:
3-bromo-6-methoxy-2-phenyl-4H-chromen-4-one is used as a pharmaceutical candidate for its potential antitumor and antiproliferative properties. It is being studied for its ability to inhibit the growth and proliferation of cancer cells, making it a valuable compound in the development of new cancer treatments.
Used in Drug Development Research:
In the field of drug development research, 3-bromo-6-methoxy-2-phenyl-4H-chromen-4-one serves as a key subject of investigation. Its unique structure and identified biological activities contribute to the exploration of new therapeutic agents, particularly those targeting cancer-related pathways and mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 215999-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,9,9 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 215999-39:
(8*2)+(7*1)+(6*5)+(5*9)+(4*9)+(3*9)+(2*3)+(1*9)=176
176 % 10 = 6
So 215999-39-6 is a valid CAS Registry Number.
215999-39-6Relevant articles and documents
An efficient synthesis of 3-bromoflavones under solvent free conditions using grinding technique
Jakhar, Komal,Makrandi
, p. 770 - 773 (2012/06/30)
Selective bromination of 1-(2-hydroxyphenyl)-3-phenylpropane- 1,3-diones has been carried out with ammonium bromide and ammonium persulphate at room temperature using grinding technique under solvent free conditions to give 2-bromo derivatives which on cyclodehydration with p-toluenesulphonic acid under grinding conditions give 3-bromoflavones. Also, flavones on bromination using above mentioned conditions give 3-bromoflavones directly.
