CAS 42870-65-5

N-Methylcycloheptanamine

Description:

N-Methylcycloheptanamine, with the CAS number 42870-65-5, is an organic compound characterized by its cyclic structure and amine functional group. It features a seven-membered cycloheptane ring with a methyl group attached to the nitrogen atom of the amine. This compound is typically colorless to pale yellow and may have a distinct odor. N-Methylcycloheptanamine is classified as an aliphatic amine, which influences its reactivity and solubility properties. It is soluble in organic solvents and may exhibit basicity due to the presence of the amine group. The compound is of interest in various chemical applications, including potential use in the synthesis of pharmaceuticals and agrochemicals. Safety data indicates that, like many amines, it may pose risks such as irritation to skin and eyes, and appropriate handling precautions should be observed. As with any chemical substance, understanding its properties and potential hazards is essential for safe use in laboratory and industrial settings.

Formula: C₈H₁₇N

InChI: InChI=1S/C8H17N/c1-9-8-6-4-2-3-5-7-8/h8-9H,2-7H2,1H3

InChI key: InChIKey=LRXSDHDEISIWQB-UHFFFAOYSA-N

SMILES: N(C)C1CCCCCC1

Synonyms:

• Cycloheptanamine, N-methyl-
• Cycloheptylamine, N-methyl-
• N-Methylcycloheptylamine
• N-cycloheptyl-N-methylamine
• NSC 123851
• N-Methylcycloheptanamine

N-Cycloheptyl-N-methylamine

CAS: 42870-65-5

Formula: C₈H₁₇N

Purity: 97%

Color and Shape: Liquid

Molecular weight: 127.2273

Ref: IN-DA00C8VN

N-Cycloheptylmethylamine

CAS: 42870-65-5

N-Cycloheptylmethylamine

Purity: 97%

Molecular weight: 127.23g/mol

Ref: 54-OR1014334

N-methylcycloheptanamine hydrochloride

CAS: 42870-65-5

Formula: C₈H₁₈ClN

Purity: 95.0%

Color and Shape: No data available.

Molecular weight: 163.69

Ref: 10-F359802

N-Methylcycloheptanamine

CAS: 42870-65-5

N-Methylcycloheptanamine (NMCA) is a pyrimidine compound that has inhibitory activities against hexamethylenetetramine and aminopeptidase. NMCA also inhibits the immunosuppressive effect of cyclophosphamide, which is an anticancer drug. NMCA has been shown to be effective in treating autoimmune diseases and cancer. The inhibitory activity of NMCA on hexamethylenetetramine and aminopeptidase is due to its ability to react with these enzymes in nanomolar concentrations. Structural analysis has shown that NMCA binds to the enzyme by coordinating with the catalytic metal ions and the amino acid residues of the active site, forming a covalent bond with glutamic acid residue. This binding prevents substrate binding or product release, inhibiting enzyme activity.

Formula: C₈H₁₇N

Purity: Min. 95%

Molecular weight: 127.23 g/mol

Ref: 3D-SBA87065