21635-88-1 | 3-Oxetanamine

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$6.00	$4.00
1g	97%	in stock	$7.00	$5.00
5g	97%	in stock	$24.00	$17.00
10g	97%	in stock	$47.00	$33.00
25g	97%	in stock	$114.00	$80.00

Description

• Catalog Number: AB46823
• Chemical Name: 3-Oxetanamine
• CAS Number: 21635-88-1
• Molecular Formula: C3H7NO
• Molecular Weight: 73.0938
• MDL Number: MFCD08544363
• SMILES: NC1COC1

Computed Properties

• Complexity: 33.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 5
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: -1

Upstream Synthesis Route

3-Oxetanamine, also known as 3-aminooxetane, is a versatile compound commonly used in chemical synthesis for its unique reactivity and structural properties. In organic synthesis, 3-oxetanamine serves as a valuable building block for the construction of complex molecules due to its ability to participate in a variety of reactions.One important application of 3-oxetanamine is its use as a precursor in the synthesis of heterocyclic compounds. By incorporating this compound into chemical reactions, chemists can access diverse molecular structures with potential pharmaceutical, agricultural, or material science applications. The presence of an amine functional group in 3-oxetanamine also enables further derivatization, allowing for the introduction of additional functionalities or stereochemical control in the target molecules.Additionally, 3-oxetanamine can serve as a chiral starting material for asymmetric synthesis. Its three-membered oxetane ring imparts unique stereochemical properties that can be leveraged to selectively generate enantiomerically pure compounds, a crucial aspect in drug discovery and other areas of medicinal chemistry. Furthermore, the strained nature of the oxetane ring provides a driving force for various ring-opening reactions, leading to the formation of diverse chemical motifs with high efficiency.Overall, the utility of 3-oxetanamine in chemical synthesis lies in its versatility, reactivity, and potential for structural diversification, making it a valuable tool for organic chemists seeking to access novel molecular architectures and functional materials.