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3,5-Dichlorphenoxy-essigsaeuremethylester, also known as 3,5-dichlorophenoxyacetic acid methyl ester, is an organic compound with the chemical formula C9H8Cl2O3. It is a derivative of 3,5-dichlorophenoxyacetic acid, where the carboxylic acid group is esterified with methanol. 3,5-Dichlorphenoxy-essigsaeuremethylester is a white crystalline solid and is used as an intermediate in the synthesis of various agrochemicals, particularly herbicides. It is known for its ability to control broadleaf and grassy weeds in agricultural settings. Due to its chemical structure, it exhibits selective herbicidal activity, which is crucial for its application in crop protection without harming the desired plant species.

1928-54-7

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1928-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1928-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1928-54:
(6*1)+(5*9)+(4*2)+(3*8)+(2*5)+(1*4)=97
97 % 10 = 7
So 1928-54-7 is a valid CAS Registry Number.

1928-54-7Relevant academic research and scientific papers

Design and Synthesis of Novel 4-Hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one Derivatives for Use as Herbicides and Evaluation of Their Mode of Action

Lei, Kang,Li, Pan,Yang, Xue-Fang,Wang, Shi-Ben,Wang, Xue-Kun,Hua, Xue-Wen,Sun, Bin,Ji, Lu-Sha,Xu, Xiao-Hua

, p. 10489 - 10497 (2019)

In order to develop a novel herbicide containing the β-triketone motif, a series of 4-hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one derivatives were designed and synthesized. The bioassay results showed that compound II15 had good pre-emergent herbicidal activity even at a dosage of 187.5 g ha-1. Moreover, compound II15 showed a broader spectrum of weed control when compared with a commercial herbicide 2,4-dichlorophenoxyacetic acid (2,4-D), and displayed good crop safety to Triticum aestivum L. and Zea mays Linn. when applied at 375 g ha-1 under pre-emergence conditions, which indicated its great potential as a herbicide. More importantly, studying the molecular mode of action of compound II15 revealed that the novel triketone structure is a proherbicide of its corresponding phenoxyacetic acid auxin herbicide, which has a herbicidal mechanism similar to that of 2,4-D. The present work indicates that the 4-hydroxyl-3-(2-phenoxyacetyl)-pyran-2-one motif may be a potential lead structure for further development of novel auxin-type herbicides.

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