CAS 5062-67-9

1-Aminocyclohexanemethanamine

Description:

1-Aminocyclohexanemethanamine, also known as cyclohexylaminomethylamine, is an organic compound characterized by its amine functional groups. It features a cyclohexane ring with an amino group and a methanamine side chain, which contributes to its basicity and potential reactivity. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in water and various organic solvents, making it versatile for different applications. The presence of multiple amine groups allows for hydrogen bonding, which can influence its physical properties and interactions with other molecules. 1-Aminocyclohexanemethanamine is often used in the synthesis of pharmaceuticals, agrochemicals, and as a building block in organic chemistry. Safety considerations include handling it with care due to its potential irritant effects on skin and mucous membranes. Proper storage and disposal methods should be followed to mitigate any environmental impact.

Formula: C₇H₁₆N₂

InChI: InChI=1/C7H16N2/c8-6-7(9)4-2-1-3-5-7/h1-6,8-9H2

InChI key: InChIKey=QCDMSCUTQSXHCU-UHFFFAOYSA-N

SMILES: C(N)C1(N)CCCCC1

Synonyms:

• Cyclohexanemethanamine, 1-amino-
• Cyclohexanemethylamine, 1-amino-
• 1-Aminocyclohexanemethylamine
• 1-Aminocyclohexanemethanamine
• 1-(Aminomethyl)cyclohexylamine
• 1-(Aminomethyl)cyclohexanamine
• (1-AMINOCYCLOHEXYL)METHYLAMINE DIHYDROCHLORIDE
• 1-Aminomethylcyclohexylamine
• 1-Aminocyclohexylmethanol (ACyHM)
• 1-(aminomethyl)cyclohexan-1-amine dihydrochloride
• 1-(Aminomethyl)cyclohexan-1-amine
• 1-amino-1-aminomethyl-cyclohexane

1-(aminomethyl)cyclohexan-1-amine

CAS: 5062-67-9

Formula: C₇H₁₆N₂

Molecular weight: 128.2153

Ref: IN-DA00DN2N

[(1-aminocyclohexyl)methyl]amine

CAS: 5062-67-9

[(1-aminocyclohexyl)methyl]amine is a white crystalline solid that is soluble in water, alcohol, and ether. It has a pKb of 2.5 and decomposes at 240°C. [(1-aminocyclohexyl)methyl]amine is an unsymmetrical molecule with two phenyl groups. This compound has been shown to catalyze the reaction between cyclohexanone and hydrophilic inorganic compounds, such as hydrochloric acid or potassium hydroxide, to form alkali metal cyclohexanones. [(1-aminocyclohexyl)methyl]amine also has antitumor activity by causing DNA damage and inhibiting protein synthesis in cancer cells.
[[File:https://upload.wikimedia.org/wikipedia/commons/thumb/2/2a/Chemical_Structures_of_Quinolones-5D4A8F87E

Formula: C₇H₁₆N₂

Purity: Min. 95%

Molecular weight: 128.22 g/mol

Ref: 3D-FAA06267