CAS 40015-92-7

2-Aminocyclohexanemethanamine

Description:

2-Aminocyclohexanemethanamine, also known as 1-amino-2-cyclohexylmethanamine, is an organic compound characterized by its amine functional groups and a cyclohexane ring structure. This compound features a primary amine (-NH2) and a secondary amine (-NH) within its molecular framework, contributing to its reactivity and potential applications in various chemical processes. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the cyclohexane ring imparts a degree of rigidity to the molecule, influencing its physical properties such as boiling point and solubility. 2-Aminocyclohexanemethanamine is of interest in the synthesis of pharmaceuticals, agrochemicals, and as a building block in organic synthesis due to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety data should be consulted for handling, as amines can be irritants and may pose health risks if not managed properly.

Formula: C₇H₁₆N₂

InChI: InChI=1S/C7H16N2/c8-5-6-3-1-2-4-7(6)9/h6-7H,1-5,8-9H2

InChI key: InChIKey=ZUYYQGFCSKJGDO-UHFFFAOYSA-N

SMILES: C(N)C1C(N)CCCC1

Synonyms:

• 1-Amino-2-aminomethylcyclohexane
• 2-(Aminomethyl)cyclohexan-1-amine
• 2-(Aminomethyl)cyclohexylamine
• 2-Aminocyclohexanemethanamine
• Cyclohexanemethanamine, 2-amino-
• 2-(Aminomethyl)cyclohexanamine

2-(Aminomethyl)cyclohexan-1-amine

CAS: 40015-92-7

2-(Aminomethyl)cyclohexan-1-amine is a synthetic compound that belongs to the group of phenethylamines. It has been shown to inhibit the growth of L1210, a murine leukemia cell line, and also shows cytotoxic effects on the HL-60 human leukemia cell line. It has shown an ability to chelate ring structures such as flavin and mononucleotide. The 2-(aminomethyl)cyclohexan-1-amine molecule can be converted into two isomers, namely 2-(aminomethyl)cyclohexanol and 2-(aminomethyl)cyclohexanone.
2-(Aminomethyl)cyclohexanol is a synthetic compound that belongs to the group of phenethylamines. It has been shown to inhibit the growth of L1210, a murine leukemia cell line, and also shows cytotoxic effects on the HL-60 human

Formula: C₇H₁₆N₂

Purity: Min. 95%

Molecular weight: 128.22 g/mol

Ref: 3D-QBA01592