CAS 39959-74-5

Benzenemethanamine, N-cyclopropyl-, hydrochloride (1:1)

Description:

Benzenemethanamine, N-cyclopropyl-, hydrochloride (1:1), also known by its CAS number 39959-74-5, is a chemical compound characterized by its amine functional group and a cyclopropyl substituent attached to a benzylamine structure. This compound typically appears as a white to off-white crystalline solid and is soluble in water due to the presence of the hydrochloride salt form, which enhances its solubility compared to the free base. The presence of the cyclopropyl group can influence its pharmacological properties, potentially affecting its interaction with biological targets. As a hydrochloride salt, it is often used in pharmaceutical formulations to improve stability and bioavailability. The compound may exhibit various biological activities, making it of interest in medicinal chemistry and drug development. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₀H₁₃N·ClH

InChI: InChI=1S/C10H13N.ClH/c1-2-4-9(5-3-1)8-11-10-6-7-10;/h1-5,10-11H,6-8H2;1H

InChI key: InChIKey=SUDZAPVGJAYJHC-UHFFFAOYSA-N

SMILES: C(NC1CC1)C2=CC=CC=C2.Cl

Synonyms:

• Benzenemethanamine, N-cyclopropyl-, hydrochloride (1:1)
• Benzenemethanamine, N-cyclopropyl-, hydrochloride

N-Cyclopropylbenzylamine HCl

CAS: 39959-74-5

Formula: C₁₀H₁₄ClN

Molecular weight: 183.6779

Ref: IN-DA00CLUE

N-Cyclopropylbenzylamine HCl

CAS: 39959-74-5

N-Cyclopropylbenzylamine HCl is a molecule that is used in the synthesis of other compounds. It is an amine that has been reconstituted and inactivated with water. N-Cyclopropylbenzylamine HCl irreversibly inhibits phosphodiesterase type 4, which catalyzes the hydrolysis of cyclic adenosine monophosphate (cAMP). The bond between the N-cyclopropyl group and the benzene ring is cleaved, yielding a residue.

Formula: C₁₀H₁₃N·HCl

Purity: Min. 95%

Molecular weight: 183.68 g/mol

Ref: 3D-PBA95974