102065-92-9 | N-(Azetidin-3-yl)acetamide hydrochloride

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$57.00	$40.00
500mg	95%	in stock	$88.00	$62.00
1g	95%	in stock	$114.00	$80.00
5g	95%	in stock	$387.00	$271.00
10g	95%	in stock	$667.00	$467.00
25g	95%	in stock	$1,319.00	$923.00

Description

• Catalog Number: AA08206
• Chemical Name: N-(Azetidin-3-yl)acetamide hydrochloride
• CAS Number: 102065-92-9
• Molecular Formula: C5H11ClN2O
• Molecular Weight: 150.6066
• MDL Number: MFCD08059477
• SMILES: CC(=O)NC1CNC1.Cl

Computed Properties

• Complexity: 98.6
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 1

Upstream Synthesis Route

N-(Azetidin-3-yl)acetamide hydrochloride is a versatile compound frequently utilized in chemical synthesis due to its unique reactivity and functional group compatibility. This compound serves as a valuable building block in the development of various organic molecules, especially in the pharmaceutical industry, where its presence in the molecular structure can enhance biological activity or modify properties such as solubility or stability. In peptide chemistry, N-(Azetidin-3-yl)acetamide hydrochloride is commonly employed as a protecting group for the amino group of amino acids during peptide synthesis. Its introduction allows for selective deprotection at a later stage, enabling site-specific modification and facilitating the assembly of complex peptide sequences with high purity and efficiency. Furthermore, this compound can participate in a range of cross-coupling reactions, including Suzuki-Miyaura, Heck, and Sonogashira reactions, leading to the formation of diverse functionalized molecules with tailored properties.The unique structural features of N-(Azetidin-3-yl)acetamide hydrochloride make it a valuable tool in the hands of synthetic chemists for the construction of intricate organic frameworks and the discovery of novel compounds for various applications in drug discovery, material science, and chemical biology.