CAS 14370-45-7

2-aminonorbornane hydrochloride

Description:

2-Aminonorbornane hydrochloride is a chemical compound characterized by its bicyclic structure, derived from norbornane, with an amino group (-NH2) attached to one of the carbon atoms. This compound is typically encountered as a hydrochloride salt, which enhances its solubility in water and makes it more stable for various applications. It is a colorless to white crystalline solid, exhibiting basic properties due to the presence of the amino group. The compound is often used in organic synthesis and as an intermediate in the production of pharmaceuticals and agrochemicals. Its unique bicyclic structure contributes to its potential as a chiral building block in asymmetric synthesis. Additionally, 2-aminonorbornane hydrochloride may exhibit biological activity, making it of interest in medicinal chemistry. Safety data indicates that, like many amines, it should be handled with care, as it may cause irritation upon contact with skin or mucous membranes. Proper storage conditions are essential to maintain its stability and prevent degradation.

Formula: C₇H₁₄ClN

InChI: InChI=1/C7H13N.ClH/c8-7-4-5-1-2-6(7)3-5;/h5-7H,1-4,8H2;1H

SMILES: C1CC2CC1CC2N.Cl

Synonyms:

• Bicyclo[2.2.1]Heptan-2-Amine
• Bicyclo[2.2.1]Heptan-2-Amine Hydrochloride (1:1)

Bicyclo[2.2.1]heptan-2-amine, hydrochloride (1:1)

CAS: 14370-45-7

Formula: C₇H₁₄ClN

Purity: 97%

Color and Shape: Solid

Molecular weight: 147.6458

Ref: IN-DA001I89

Exo-norbornylamine hydrochloride

CAS: 14370-45-7

Exo-norbornylamine hydrochloride

Purity: 95%

Color and Shape: Powder

Molecular weight: 147.65g/mol

Ref: 54-OR945288

Exo-norbornylamine hydrochloride

CAS: 14370-45-7

Exo-norbornylamine hydrochloride is a metabolite of amantadine and is produced by acetylation of the aromatic ring. It has been shown to be a substrate for epoxide hydrolase, which catalyzes the conversion of this compound to an epoxide. It has been shown to inhibit influenza virus replication in vitro and in vivo, possibly by regulating ion channels or inhibiting viral RNA synthesis. Exo-norbornylamine hydrochloride also inhibits lung epithelial cell proliferation, which may be due to its ability to inhibit the production of inflammatory mediators such as prostaglandins and leukotrienes.

Formula: C₇H₁₃N·HCl

Purity: Min. 95%

Molecular weight: 147.65 g/mol

Ref: 3D-PAA37045