1036260-25-9 | 3-Aminocyclobutanol hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$12.00	$9.00
250mg	98%	in stock	$17.00	$12.00
1g	98%	in stock	$52.00	$37.00
5g	98%	in stock	$239.00	$168.00

Description

• Catalog Number: AE11612
• Chemical Name: 3-Aminocyclobutanol hydrochloride
• CAS Number: 1036260-25-9
• Molecular Formula: C4H10ClNO
• Molecular Weight: 123.5813
• MDL Number: MFCD12547215
• SMILES: NC1CC(C1)O.Cl

Upstream Synthesis Route

3-Aminocyclobutanol hydrochloride is a versatile compound widely utilized in chemical synthesis for its unique properties and functionalities. This compound serves as a valuable building block in the production of various organic molecules due to its ability to undergo diverse chemical reactions and transformations. In particular, 3-Aminocyclobutanol hydrochloride is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.One key application of 3-Aminocyclobutanol hydrochloride in chemical synthesis is its use as a chiral building block for the creation of enantiopure compounds. The presence of a chiral center in the molecule allows for the formation of stereochemically pure products, making it a crucial component in asymmetric synthesis strategies. By incorporating 3-Aminocyclobutanol hydrochloride into the reaction pathway, chemists can efficiently access enantiomerically pure compounds with high levels of selectivity and yield.Additionally, 3-Aminocyclobutanol hydrochloride can also act as a nucleophilic reagent in various organic transformations. Its nucleophilic nature enables it to participate in reactions such as substitution, addition, and ring-opening reactions, leading to the formation of complex molecular structures. This versatility makes 3-Aminocyclobutanol hydrochloride a valuable tool for chemists working on the synthesis of intricate organic molecules with specific functional groups and stereochemical arrangements.Furthermore, the structural characteristics of 3-Aminocyclobutanol hydrochloride make it an ideal precursor for the synthesis of heterocyclic compounds and bioactive molecules. Its cyclobutane ring scaffold offers opportunities for cyclization reactions, enabling the construction of diverse ring systems found in natural products and pharmaceutical agents. This versatility in ring-forming reactions further highlights the significance of 3-Aminocyclobutanol hydrochloride in the realm of chemical synthesis, particularly in the development of novel drug candidates and fine chemicals.