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3-Nitro-4-propyl-acetophenone is an organic compound with the chemical formula C11H13NO3. It is a derivative of acetophenone, featuring a nitro group at the 3rd carbon position and a propyl group at the 4th carbon position. This yellow crystalline substance is soluble in organic solvents and has a molecular weight of 207.23 g/mol. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its reactivity, it is essential to handle 3-nitro-4-propyl-acetophenone with care, as it may pose health risks and environmental concerns.

2932-64-1

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2932-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2932-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2932-64:
(6*2)+(5*9)+(4*3)+(3*2)+(2*6)+(1*4)=91
91 % 10 = 1
So 2932-64-1 is a valid CAS Registry Number.

2932-64-1Relevant academic research and scientific papers

Dichloroacetophenones targeting at pyruvate dehydrogenase kinase 1 with improved selectivity and antiproliferative activity: Synthesis and structure-activity relationships

Zhang, Shao-Lin,Yang, Zheng,Hu, Xiaohui,Tam, Kin Yip

supporting information, p. 3441 - 3445 (2018/09/29)

Dichloroacetophenone is a pyruvate dehydrogenase kinase 1 (PDK1) inhibitor with suboptimal kinase selectivity. Herein, we report the synthesis and biological evaluation of a series of novel dichloroacetophenones. Structure-activity relationship analyses (SARs) enabled us to identify three potent compounds, namely 54, 55, and 64, which inhibited PDK1 function, activated pyruvate dehydrogenase complex, and reduced the proliferation of NCI-H1975 cells. Mitochondrial bioenergetics assay suggested that 54, 55, and 64 enhanced the oxidative phosphorylation in cancer cells, which might contribute to the observed anti-proliferation effects. Collectively, these results suggested that 54, 55, and 64 could be promising compounds for the development of potent PDK1 inhibitors.

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