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3-(4'-Chlorobenzylidene)benzofuran-2(3H)-one is a chemical compound with the molecular formula C15H9ClO2. It is a derivative of benzofuran, a heterocyclic aromatic organic compound consisting of a benzene ring fused to a furan ring. The compound features a 4'-chlorobenzylidene group attached to the benzofuran core, which introduces a chlorine atom at the para position of the benzylidene moiety. This chemical structure may exhibit various biological activities and can be used in the synthesis of pharmaceuticals, agrochemicals, or other organic compounds. Due to its specific functional groups and molecular arrangement, it may have potential applications in the field of materials science, medicinal chemistry, and chemical research.

1025-49-6

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1025-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1025-49:
(6*1)+(5*0)+(4*2)+(3*5)+(2*4)+(1*9)=46
46 % 10 = 6
So 1025-49-6 is a valid CAS Registry Number.

1025-49-6Upstream product

1025-49-6Relevant academic research and scientific papers

Benzobutyrolactone derivatives, synthetic method and application thereof in preparation of bactericides

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Paragraph 0049; 0050; 0051; 0056, (2018/04/03)

The invention discloses benzobutyrolactone derivatives, a synthetic method and application thereof in preparation of bactericides. The method comprises the following steps: taking sesquiterpene lactone pharmacophore alpha-methylene-gamma-butyrolactone as a lead compound, integrating benzofuranone pharmacophore, modifying at an alpha-methylene position, and performing directional derivative synthesis to obtain a series of alpha-alkenylene benzobutyrolactone compounds. The antibacterial activities of the compounds are determined, and two high-activity compounds with excellent industrialization development prospects are synthesized on the structure-effect basis. The compounds are used for controlling plant diseases caused by pathogenic bacteria such as wheat powdery mildew, wheat scab, take-all disease of wheat, wheat sharp eyespot, corn northern leaf blight, rice sheath blight disease, rice blast, cotton damping-off, phytoph-thora capsici leonian, botrytis cinerea, tomato leaf mould, tomato early/late blight, cucumber anthracnose, fusarium wilt of cucumber, sclerotinia rot of colza and the like.

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