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1,2-Benzisoxazole, 5-bromo-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

402914-15-2

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402914-15-2 Usage

Structure

Benzisoxazole derivative with a bromine atom at the third carbon and a phenyl group at the second carbon

Explanation

The compound is derived from benzisoxazole, which is a fused ring system consisting of a benzene ring and an isoxazole ring. The bromine atom is attached to the third carbon atom of the isoxazole ring, and the phenyl group is attached to the second carbon atom of the benzene ring.

Explanation

Due to its versatile reactivity and structural properties, 1,2-Benzisoxazole, 5-bromo-3-phenylis used as a starting material or intermediate in the synthesis of various organic compounds and pharmaceuticals.

Explanation

The compound's unique structure and reactivity make it a promising candidate for the development of new drugs and agrochemicals, which can have various applications in medicine and agriculture.

Explanation

Studies have shown that 1,2-Benzisoxazole, 5-bromo-3-phenylmay have potential biological activities, such as inhibiting specific enzymes and receptors. This property could be useful in the development of drugs targeting these biological targets.

Explanation

The compound's reactivity is influenced by the presence of the bromine atom and the phenyl group, which can participate in various chemical reactions, such as substitution, addition, and elimination reactions.

Explanation

The unique structure of the compound, consisting of a fused benzene and isoxazole ring system, contributes to its reactivity and potential applications in various fields.

Applications

Building block in organic synthesis and pharmaceutical research

Potential Applications

Development of pharmaceutical and agrochemical products

Biological Activities

Inhibition of certain enzymes and receptors in the human body

Reactivity

Versatile reactivity

Structural Properties

Fused benzene and isoxazole rings

Check Digit Verification of cas no

The CAS Registry Mumber 402914-15-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,9,1 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 402914-15:
(8*4)+(7*0)+(6*2)+(5*9)+(4*1)+(3*4)+(2*1)+(1*5)=112
112 % 10 = 2
So 402914-15-2 is a valid CAS Registry Number.

402914-15-2Downstream Products

402914-15-2Relevant academic research and scientific papers

METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION

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Paragraph 0228; 0229, (2022/01/06)

Mutations in oncogenes and tumor suppressors contribute to the development and progression of cancer. The present disclosure describes compounds and methods that restore DNA binding affinity of p53 mutants. The compounds of the present disclosure can bind to mutant p53 and restore the ability of the p53 mutant to bind DNA and activate downstream effectors involved in tumor suppression. The disclosed compounds can be used to reduce the progression of cancers that contain a p53 mutation.

SUBSTITUTED BENZOFURAN COMPOUNDS AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES

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Page/Page column 68; 69, (2013/03/26)

The present invention relates to compounds of formula (I) that are useful as hepatitis C virus (HCV) NS5B polymerase inhibitors, the synthesis of such compounds, and the use of such compounds for inhibiting HCV NS5B polymerase activity, for treating or preventing HCV infections and for inhibiting HCV viral replication and/or viral production in a cell-based system.

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