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1-(2-fluoro-phenyl)-propane-1,2-dione-2-oxime is a chemical compound with the molecular formula C9H7FNO2. It is a derivative of 1-phenylpropane-1,2-dione (also known as benzoyl acetone), where one of the hydrogen atoms on the phenyl ring is replaced by a fluorine atom, and the oxime group is attached to the carbonyl carbon. 1-(2-fluoro-phenyl)-propane-1,2-dione-2-oxime is characterized by its fluorinated aromatic structure and oxime functionality, which can be relevant in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The presence of the fluorine atom can significantly influence the compound's reactivity, stability, and physical properties, making it a potentially valuable intermediate in organic synthesis.

389-41-3

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389-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 389-41-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 389-41:
(5*3)+(4*8)+(3*9)+(2*4)+(1*1)=83
83 % 10 = 3
So 389-41-3 is a valid CAS Registry Number.

389-41-3Upstream product

389-41-3Downstream Products

389-41-3Relevant academic research and scientific papers

Nitrosocarbonyl-Henry and Denitration Cascade: Synthesis of α-Ketoamides and α-Keto Oximes

Reddy, Mallu Kesava,Mallik, Sumitava,Ramakrishna, Isai,Baidya, Mahiuddin

, p. 1694 - 1697 (2017)

An unprecedented Henry reaction of in situ generated nitrosocarbonyl intermediates and concomitant denitration cascade has been developed. The reaction is catalyzed by organic base at room temperature offering α-ketoamides, a demanding scaffold for drug discovery, in high yields. An alteration of substitution pattern also produced α-keto oximes, a high-value synthon. The protocol features operational simplicity and broad substrate scope.

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