CAS 16315-16-5

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one

Description:

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one, with the CAS number 16315-16-5, is a heterocyclic organic compound characterized by its indazole structure, which features a fused ring system containing nitrogen atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents, reflecting its non-polar characteristics. The presence of multiple methyl groups contributes to its hydrophobic nature and can influence its reactivity and interactions with biological systems. It is often studied for its potential applications in pharmaceuticals and agrochemicals due to its unique structural properties. The compound's molecular framework allows for various functionalization possibilities, making it a subject of interest in synthetic organic chemistry. Additionally, its stability and reactivity can be influenced by the presence of substituents on the indazole ring, which may affect its biological activity and potential therapeutic uses. Overall, 3,6,6-Trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one represents a versatile compound in the realm of organic synthesis and medicinal chemistry.

Formula: C₁₀H₁₄N₂O

InChI: InChI=1/C10H14N2O/c1-6-9-7(12-11-6)4-10(2,3)5-8(9)13/h4-5H2,1-3H3,(H,11,12)

SMILES: Cc1c2c(CC(C)(C)CC2=O)n[nH]1

Synonyms:

• 4H-Indazol-4-one, 1,5,6,7-tetrahydro-3,6,6-trimethyl

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one

CAS: 16315-16-5

Formula: C₁₀H₁₄N₂O

Color and Shape: Solid

Molecular weight: 178.2310

Ref: IN-DA001TTQ

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4h-indazol-4-one

CAS: 16315-16-5

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4h-indazol-4-one

Purity: 97%

Molecular weight: 178.23g/mol

Ref: 54-OR929611

3,6,6-Trimethyl-1,5,6,7-tetrahydro-4h-indazol-4-one

CAS: 16315-16-5

Isoxazoles are a class of chemical compounds that contain the isoxazole ring. Isoxazoles can be synthesized by ring-opening reactions from 1,3-dihydroisoxazol-2-ones or by the reductive condensation of 2-hydroxybenzaldehydes and malononitrile derivatives. The synthesis of 3,6,6-trimethyl-1,5,6,7-tetrahydro-4H-indazol-4-one (TMI) is an example of this type of reaction. This compound was prepared in 1949 by H.P. Brown and coworkers at DuPont as part of their search for an organic insecticide. TMI has been shown to have a high degree of stability across a range of conditions and temperatures.

Formula: C₁₀H₁₄N₂O

Purity: Min. 95%

Molecular weight: 178.24 g/mol

Ref: 3D-RAA31516