ChemicalBook--->CAS DataBase List--->3176-62-3

3176-62-3

3176-62-3 Structure

3176-62-3 Structure
IdentificationBack Directory
[Name]

3-METHYL-1H-INDAZOLE
[CAS]

3176-62-3
[Synonyms]

3-METHYL-1H-INDAZOLE
1H-Indazole, 3-methyl-
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C8H8N2
[MDL Number]

MFCD00601361
[MOL File]

3176-62-3.mol
[Molecular Weight]

132.16
Chemical PropertiesBack Directory
[Melting point ]

113°C
[Boiling point ]

234.08°C (rough estimate)
[density ]

1.1083 (rough estimate)
[refractive index ]

1.6013 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

14.39±0.40(Predicted)
[InChI]

InChI=1S/C8H8N2/c1-6-7-4-2-3-5-8(7)10-9-6/h2-5H,1H3,(H,9,10)
[InChIKey]

FWOPJXVQGMZKEP-UHFFFAOYSA-N
[SMILES]

N1C2=C(C=CC=C2)C(C)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H317-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2933998090
Hazard InformationBack Directory
[Description]

3-Methyl-1H-indazole is a heterocyclic alkyl compound containing nitrogen and three methyl groups. It is used as an intermediate in the synthesis of other compounds. It has been shown to have anti-inflammatory properties in vitro. It also inhibits neutrophil chemotaxis and may be used to treat inflammatory diseases such as trigeminal neuralgia or heart disease. 3-Methyl-1H-indazole has also been shown to inhibit histamine H3 receptor activity, which may account for its effects on eye diseases and bladder cancer.
[Uses]

3-Methyl-1H-indazole is an intermediate compound. It can be used as an organic synthesis reagent for the preparation of 3-methyl-1H-indazol-5-amine and 3-methyl-5-nitro-1H-indazole compounds. In addition, the 3-Methyl-1H-indazole derivatives (1a-1d and 2a-2d) have antimicrobial effects, both having antibacterial activity against Bacillus subtilis and Escherichia coli[1].
[Synthesis Reference(s)]

Journal of Heterocyclic Chemistry, 25, p. 1817, 1988 DOI: 10.1002/jhet.5570250641
Synthesis, p. 982, 1984
[References]

[1] FARRUKH SHAIKH. Synthesis and evaluation of antibacterial activity of novel 3-methyl-1H-indazole derivatives[J]. Intelligent Pharmacy, 2024. DOI:10.1016/j.ipha.2023.09.003.
Spectrum DetailBack Directory
[Spectrum Detail]

3-METHYL-1H-INDAZOLE(3176-62-3)1HNMR
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