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1353119-32-0

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1353119-32-0 Usage

General Description

The chemical compound "(2Z)-2-(3-fluorobenzylidene)-6-hydroxy-1-benzofuran-3(2H)-one" is a benzofuran derivative with a hydroxy group and a fluorobenzylidene substituent. It belongs to the class of organic compounds known as benzofurans, which are compounds containing a benzene ring fused to a furan ring. This specific compound has a hydroxy group at position 6 and a fluorobenzylidene group attached to position 2 of the benzofuran ring. It is used in organic synthesis and chemical research, and its properties and potential applications may be of interest to scientists and researchers in the field of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 1353119-32-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,3,1,1 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1353119-32:
(9*1)+(8*3)+(7*5)+(6*3)+(5*1)+(4*1)+(3*9)+(2*3)+(1*2)=130
130 % 10 = 0
So 1353119-32-0 is a valid CAS Registry Number.

1353119-32-0Downstream Products

1353119-32-0Relevant articles and documents

Synthesis and Biological Activities of 6-Hydroxyaurone Derivatives

Bao, Yong-Tuan,Zhang, Min,Li, Ting,Xiao, Hui-Feng,Zhao, Ting,Xu, Xiao-Hua,Yang, Liu-Qing

, p. 637 - 642 (2016)

A series of 6-hydroxyaurone derivatives were synthesized in satisfactory yields and characterized by IR, 1H NMR, 13C NMR, and HRMS or elemental analysis. The structure of compound 3e was further confirmed by X-ray crystal analysis. B

6-aryloxyacetic acetoxy orange ketones compound and the application of the pesticides

-

, (2016/12/01)

The invention relates to a 6-aryloxy acetoxy aurone compound and an application thereof on a pesticide, and belongs to the technical field of herbicides. The general formula of the 6-aryloxy acetoxy aurone compound is as shown in the specification, wherein R1 is hydrogen, halogen, C1-C4 haloalkyl, C1-C4 alkyl, C1-C4 alkoxy and C1-C4 alkylamino, and R2 is the hydrogen and the C1-C4 alkyl. The invention provides a lot of novel chemical structures and novel compounds. A biological activity measurement result indicates that the compound I has very high weeding activity.

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