23856-15-7

Basic information

• Product Name: (5-nitro-1H-indazol-1-yl)(phenyl)methanone
• Synonyms: (5-nitro-1H-indazol-1-yl)(phenyl)methanone
• CAS NO: 23856-15-7
• Molecular Weight: 267.244
• Mol File: 23856-15-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (5-nitro-1H-indazol-1-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-nitro-1H-indazol-1-yl)(phenyl)methanone(23856-15-7)
• EPA Substance Registry System: (5-nitro-1H-indazol-1-yl)(phenyl)methanone(23856-15-7)

Safety Data

• Hazardous Substances Data: 23856-15-7(Hazardous Substances Data)

Usage

General Description

The chemical (5-nitro-1H-indazol-1-yl)(phenyl)methanone is a compound with the molecular formula C14H9N3O3. It has a nitro group and a phenyl group attached to an indazole ring. This chemical is commonly used in pharmaceutical research and drug development due to its potential biological and pharmacological activities. It may have applications in the development of new drugs for various medical conditions, including cancer and inflammatory diseases. It is important to handle this compound with care, as it may have potential hazards and should be used in accordance with proper safety protocols.

Upstream product

• 98-82-8 Isopropylbenzene 
• 99-52-5 2-methyl-4-nitro-benzenamine 
• 98-88-4 benzoyl chloride 
• 5401-94-5 5-nitroindazole 
• 93-97-0 benzoic acid anhydride 
• 857774-64-2 2-benzoyl-5-nitro-2H-indazole 

Downstream Products

• 23856-17-9 1-Benzoyl-5-amino-1H-indazol 

Relevant articles and documents

Synthesis of N-arylindazole-3-carboxamide and N-benzoylindazole derivatives and their evaluation against α-MSH-stimulated melanogenesis

We have designed and synthesized twenty-six N-arylindazole-3-carboxamide (3a-p) and N-benzoylindazole (6a-j) derivatives to discover with excellent inhibition activities of α-MSH-stimulated melanogenesis. In the bio evaluation studies of these compounds,

Reissert Compound Formation with Fused Five-Membered Ring Heterocycles

Reissert compounds have been prepared in high yield from benzothiazole by use of trimethylsilyl cyanide as source of cyanide in a single phase system.Analogues have been made from benzoxazole, indazole and 1-methylindazole but the method was unsuccessful with 1,2-benzisoxazole and pyrazole.Conjugate base alkylation followed by removal of the Reissert grouping provides a route to 2-alkylbenzothiazoles and -benzoxazoles, and 3-alkylated indazoles.Efficient access to pyridobenzothiazole and benzothiazoloisoquinoline derivatives results from appropriate intramolecular cyclisations.A crystal structure determination of 3-benzoyl-2,3-dihydro-2-benzothiazolecarbonitrile is reported.