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4-<α-(2-Methoxy-phenoxy)-acetoxy>-cumarin is a complex organic compound with the molecular formula C17H14O6. It is a derivative of coumarin, a naturally occurring organic compound found in many plants. This specific compound features a coumarin core with a 2-methoxy-phenoxy group attached to the α-carbon of an acetoxy group. The presence of the methoxy group and the acetoxy group on the phenoxy ring contributes to its unique chemical properties and potential applications. It is often used in the synthesis of various pharmaceuticals and agrochemicals due to its ability to modify the activity of the parent coumarin molecule. The compound's structure allows for a range of biological activities, making it a valuable intermediate in the development of new drugs and chemical compounds.

7548-37-0

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7548-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7548-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7548-37:
(6*7)+(5*5)+(4*4)+(3*8)+(2*3)+(1*7)=120
120 % 10 = 0
So 7548-37-0 is a valid CAS Registry Number.

7548-37-0Downstream Products

7548-37-0Relevant 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 (2019/10/02)

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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