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2-Propen-1-one, 1-(5-bromo-2-hydroxyphenyl)-3-(4-methoxyphenyl)- is a complex organic compound with the chemical formula C15H13BrO3. It is a derivative of chalcone, a type of open-chain flavonoid, characterized by the presence of a 5-bromo-2-hydroxyphenyl group and a 4-methoxyphenyl group attached to the propenone core. This molecule exhibits a unique structure, with a carbonyl group at the 1-position, a double bond between the 2nd and 3rd carbons, and a bromine atom at the 5-position of the hydroxyphenyl group. The 4-methoxyphenyl group is attached to the 3rd carbon, providing additional functionality and potential for further chemical reactions. 2-Propen-1-one, 1-(5-bromo-2-hydroxyphenyl)-3-(4-methoxyphenyl)- may have applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals due to its diverse functional groups and unique structure.

1776-04-1

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1776-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1776-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1776-04:
(6*1)+(5*7)+(4*7)+(3*6)+(2*0)+(1*4)=91
91 % 10 = 1
So 1776-04-1 is a valid CAS Registry Number.

1776-04-1Relevant academic research and scientific papers

Piperidine-mediated annulation of 2-acylphenols with 4-nitrobenzaldehyde to 3-benzofuranones

Verma, Nishant,Kundi, Varun,Ahmed, Naseem

supporting information, p. 4175 - 4179 (2015/06/22)

Piperidine - mediated reactions of 2-acylphenols and 4-nitrobenzaldehydes afforded 3-benzofuranones in high yield (82-95%) at reflux temperature in ethanol. The electron density calculation of HOMO-LUMO energy in the chalcone intermediates by DFT showed t

Synthesis and biological activities of some flavones

Sawant,Gill,Nirwan

, p. 297 - 300 (2013/09/24)

Chalcones are synthesized by a base catalyzed Claisen Schmidt condensation reaction and then treated with dimethylsulphoxide in presence of iodine to get flavones. The synthesized compounds were evaluated for their antibacterial activity against Escherichia coli, P. aeruginosa, S. epidermidis and B. subtilis. All the flavones showed moderate to good activity. The structures of these compounds were confirmed by IR, UV, 1H NMR, Mass and elemental analysis.

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