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1-(2-Methoxy-phenoxy)-propan-2-one oxime is an organic compound with the chemical formula C10H13NO3. It is a derivative of acetophenone, featuring a methoxy group attached to the phenyl ring and an oxime functional group. 1-(2-Methoxy-phenoxy)-propan-2-one oxime is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides. The presence of the oxime group endows it with unique reactivity, making it a valuable building block in organic chemistry. Its structure and properties make it a subject of interest for researchers in the field of chemical synthesis and drug development.

6437-45-2

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6437-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6437-45-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6437-45:
(6*6)+(5*4)+(4*3)+(3*7)+(2*4)+(1*5)=102
102 % 10 = 2
So 6437-45-2 is a valid CAS Registry Number.

6437-45-2Relevant academic research and scientific papers

Design, synthesis and effect of the introduction of a propargyloxy group on the fungicidal activities of 1-substituted phenoxypropan-2-amino valinamide carbamate derivatives

Li, Jian-Qiang,Wang, Zhi-Peng,Gao, Yang,Zhao, Wei-Guang

, p. 82131 - 82137 (2016/09/09)

The cell walls of oomycetes are composed of cellulose, making cellulose synthase enzymes good targets for carboxylic acid amide fungicides. Valinamide carbamates are amino acid fungicides that represent excellent alternatives to conventional synthetic pesticides in terms of their ability to reduce the negative impacts of these compounds on human health and the environment. In a continuation of our research towards the development of new cellulose synthase inhibitors, we have developed a series of "stretched" analogues of iprovalicarb by the introduction of an additional OCH2 linker. The bioassay results indicated that compounds containing a small group at the para-position of phenyl gave excellent fungicidal activities with EC50 values ranging from 0.59 to 2.06 μmol L-1. Most notably, the introduction of a propargyloxy group led to a pronounced increase in the fungicidal activity. Furthermore, compound 7o bearing a propargyloxy group was identified as the most promising candidate because of its excellent fungicidal potency against oomycete diseases and good fungicidal activity against non-oomycete diseases.

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