CAS 446866-62-2

N-methyl-1H-pyrazol-3-amine

Description:

N-methyl-1H-pyrazol-3-amine is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a methyl group attached to the nitrogen atom at the first position and an amino group at the third position of the pyrazole ring. It is typically a solid at room temperature and is soluble in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. N-methyl-1H-pyrazol-3-amine is of interest in various fields, including medicinal chemistry, where it may serve as a building block for the synthesis of biologically active compounds. Its reactivity is influenced by the electron-donating methyl group and the electron-withdrawing nature of the pyrazole ring, making it a versatile intermediate in organic synthesis. Additionally, the compound's properties, such as melting point, boiling point, and specific reactivity, can vary based on the conditions under which it is synthesized and handled.

N-Methyl-1H-pyrazol-3-amine

CAS: 446866-62-2

Formula: C₄H₇N₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 97.1185

Ref: IN-DA00E63R

N-Methyl-1H-pyrazol-3-amine

CAS: 446866-62-2

Formula: C₄H₇N₃

Purity: 95.0%

Color and Shape: Solid, Oil

Molecular weight: 97.121

Ref: 10-F450317

N-Methyl-1h-pyrazol-3-amine

CAS: 446866-62-2

N-Methyl-1h-pyrazol-3-amine is an anti-cancer drug that is used for the treatment of various types of cancer. The drug is a hydroxylamine derivative and reacts with chlorides to form N-methylhydroxamic acid chloride, which can be used to produce other bioactive molecules. This reaction mechanism may involve a cross-coupling reaction between an N atom in the nuclei and a reactive functional group on the molecule. The product of this reaction has two chlorine atoms and a symmetric carbon framework.

Purity: Min. 95%

Ref: 3D-WSA86662