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1-(5-bromo-2-hydroxy-phenyl)-3-pyridin-3-yl-propenone is a complex organic compound characterized by its molecular formula C15H10BrNO2. 1-(5-bromo-2-hydroxy-phenyl)-3-pyridin-3-yl-propenone features a 3-pyridin-3-yl-propenone core, which is a derivative of the pyridine ring system, with a 5-bromo-2-hydroxy-phenyl group attached to it. The presence of a bromine atom at the 5-position of the phenyl ring and a hydroxyl group at the 2-position introduces unique chemical properties and reactivity. This molecule is of interest in the field of organic chemistry, potentially for its applications in the synthesis of pharmaceuticals or other specialty chemicals. Its structure provides a platform for further functionalization and exploration of its chemical behavior.

1025-61-2

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1025-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1025-61:
(6*1)+(5*0)+(4*2)+(3*5)+(2*6)+(1*1)=42
42 % 10 = 2
So 1025-61-2 is a valid CAS Registry Number.

1025-61-2Relevant academic research and scientific papers

Development of novel pesticides based on phytoalexins: Part 2. Quantitative structure-activity relationships of 2-heteroaryl-4-chromanone derivatives

Yang, Guangfu,Jiang, Xiaohua,Yang, Huazheng

, p. 1063 - 1067 (2007/10/03)

Phytoalexins are low-molecular-weight chemicals that immune systems of plants produce and accumulate in response to infections, especially those of fungal origin. Although their content is not high in plants, yet they have shown unique fungicidal activity

Synthesis of pyridine and quinoline analogs of chalcone. Study of their structure by the PMR method

Khilya,Bondarenko,Turov

, p. 587 - 591 (2007/10/03)

Substituted pyridine and 2-quinoline analogs of chalcone have been synthesized. The homonuclear Overhauser effect has been used to assign the PMR signals of the olefinic protons of the indicated pyridine derivatives and to elucidate their steric orientati

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