10523-68-9 | 2-Adamantanamine, HCl

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$10.00	$7.00
500mg	97%	in stock	$15.00	$10.00
1g	97%	in stock	$18.00	$12.00
5g	97%	in stock	$20.00	$14.00
10g	97%	in stock	$39.00	$28.00

Description

• Catalog Number: AB60925
• Chemical Name: 2-Adamantanamine, HCl
• CAS Number: 10523-68-9
• Molecular Formula: C10H18ClN
• Molecular Weight: 187.7096
• MDL Number: MFCD00074743
• SMILES: NC1C2CC3CC1CC(C2)C3.Cl

Computed Properties

• Complexity: 148
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2

Upstream Synthesis Route

Adamantan-2-amine hydrochloride, a crystalline compound with the chemical formula C10H18ClN, plays a crucial role in chemical synthesis as a versatile building block. This unique compound serves as a valuable precursor in the creation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, Adamantan-2-amine hydrochloride is often used as a key intermediate in the development of specialized drugs and advanced materials due to its stable and reactive nature. Its three-dimensional structure, derived from the adamantane core, imparts specific functional properties that are highly sought after in the field of medicinal chemistry.Furthermore, Adamantan-2-amine hydrochloride is employed in the preparation of complex molecules through a series of sequential reactions that exploit its selective reactivity and compatibility with diverse chemical transformations. Its presence as a pivotal reagent enables the synthesis of intricate molecular architectures that are not readily accessible using conventional methods.Overall, the application of Adamantan-2-amine hydrochloride in chemical synthesis exemplifies its significance and utility as a strategic building block for the construction of molecular entities with tailored functionalities and potential applications across various scientific disciplines.

Literature

• Comparisons of the influenza virus A M2 channel binding affinities, anti-influenza virus potencies and NMDA antagonistic activities of 2-alkyl-2-aminoadamantanes and analogues.

  Bioorganic & medicinal chemistry letters 20081201

• [DNA macroarray analysis of gene expression changes in rat brain after single administration of 2-aminoadamantane compound].

  Molekuliarnaia biologiia 20050101