75844-28-9

Basic information

• Product Name: 6-AMINO-5-METHYLINDOLE
• Synonyms: 6-AMINO-5-METHYLINDOLE;6-AMino-5-Methyl-1H-indazole;5-Methyl-6-amino-1H-indazole;6-Amino-5-methylindazole;5-methyl-1H-Indazol-6-amine
• CAS NO: 75844-28-9
• Molecular Formula: C9H10N2
• Molecular Weight: 146.1891
• Mol File: 75844-28-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 241-242℃
• Boiling Point: 374.0±22.0 °C(Predicted)
• Appearance: /
• Density: 1.295
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 15.83±0.40(Predicted)
• CAS DataBase Reference: 6-AMINO-5-METHYLINDOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINO-5-METHYLINDOLE(75844-28-9)
• EPA Substance Registry System: 6-AMINO-5-METHYLINDOLE(75844-28-9)

Safety Data

• Hazardous Substances Data: 75844-28-9(Hazardous Substances Data)

Usage

General Description

6-AMINO-5-METHYLINDOLE is a chemical compound with the molecular formula C9H9N2, and it is a derivative of indole. 6-AMINO-5-METHYLINDOLE is primarily used in research and pharmaceutical applications, including as a building block in the synthesis of various pharmaceuticals and organic compounds. It has a molecular weight of 147.18 g/mol and a melting point of 189-190 °C. 6-AMINO-5-METHYLINDOLE has potential applications in the development of new drugs and in chemical research due to its unique structure and properties. However, it is important to handle this compound with care, as it may pose health hazards if not handled properly.

Upstream product

• 95-68-1 2,4-Xylidine 
• 2124-47-2 5-nitro-2,4-dimethylaniline 
• 72521-00-7 5-methyl-6-nitro-1H-indazole 
• 72521-00-7 5-methyl-6-nitro-1⁽²⁾H-indazole 

Downstream Products

• 78416-49-6 7-Amino-1,6-dihydro-5H-pyrazolo<4,3-g>chinazolin-5-on 
• 73908-01-7 pyrazolo<4,3-g>quinazoline-5,7-dione 
• 71785-46-1 1,6-Dihydro-5H-pyrazolo<4,3-g>chinazolin-5-on 

Relevant articles and documents

Bicyclic heterocyclic anthranilic diamides as ryanodine receptor modulators with insecticidal activity

The diamide insecticides act on the ryanodine receptor (RyR). The synthesis of various bicyclic anthranilic derivatives is reported. Their activity against the insect ryanodine receptor (RyR) and their insecticidal activity in the greenhouse is presented,

Lin-benzoaminopurinols

Novel benzologs or pyrazolo-quinazoline derivatives of the formula (I) STR1 wherein X and Y are independently selected from oxygen, sulphur and imino and wherein ring (C) is a pyrazole ring fused to ring (B) via one of the three ortho positions or sides of ring (B); the fused pyrazole ring (C) is either in the 4,3- or the 3,4-arrangement; and tautomers of formula (I) compounds; when X is not oxygen, i.e. stands for sulphur or imino, Y may stand for a covalent bond that links the hydrogen directly to the carbon atom in position 2. Two methods for producing the novel formula (I) compounds are disclosed. The first or indazole method starts from a precursor having a benzene moiety (ring B) and a pyrazolo moiety (ring C) fused therewith, i.e. the indazole structure; ring (B) carries two vicinal substituents for forming the pyrimidine moiety or ring (A) by cyclization. The second or quinazoline method starts from a precursor having the pyrimidine moiety (A) and the benzene moiety (B) fused therewith, i.e. the quinazoline structure, and carrying two vicinal substituents for forming the pyrazole moiety (C) by cyclization. The first method, in addition to yielding the novel benzologs, provides for improved synthesis of previously disclosed benzo-allopurinols. Novel compounds of formula (I) are benzologs of such well known and biologically active compounds as oxipurinol, aminopurinol and thiopurinol and are expected to be applicable for comparable pharmaceutical purposes.