15231-41-1 | tert-Butyl 3-aminopropanoate

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$13.00	$9.00
250mg	97%	in stock	$16.00	$11.00
1g	>97%	in stock	$25.00	$17.00
10g	>97%	in stock	$143.00	$100.00

Description

• Catalog Number: AD51801
• Chemical Name: tert-Butyl 3-aminopropanoate
• CAS Number: 15231-41-1
• Molecular Formula: C7H15NO2
• Molecular Weight: 145.1995
• MDL Number: MFCD06212562
• SMILES: NCCC(=O)OC(C)(C)C

Computed Properties

• Complexity: 115
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 0.1

Upstream Synthesis Route

Tert-Butyl 3-aminopropanoate is a versatile compound widely used in chemical synthesis for its unique reactivity and structural features. Its primary application lies in the field of organic chemistry, where it serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.Due to its tert-butyl ester functionality and amino group, tert-Butyl 3-aminopropanoate offers a range of synthetic possibilities. It can undergo nucleophilic substitution reactions, allowing for the introduction of different functional groups at the amino and ester positions. This reactivity makes it a valuable intermediate in the preparation of complex organic molecules.In addition, tert-Butyl 3-aminopropanoate can also participate in condensation reactions to form peptide bonds. This property is particularly important in peptide synthesis, where the compound can be employed as a protected amino acid derivative for the assembly of peptide chains with high efficiency and selectivity.Overall, tert-Butyl 3-aminopropanoate plays a crucial role in the development of new chemical entities and the exploration of diverse chemical space in modern synthesis strategies. Its versatility and reactivity make it a valuable tool for organic chemists seeking to access structurally complex molecules for various applications.

Literature

• Syntheses and bioactivities of substituted 9,10-dihydro-9,10-[1,2]benzenoanthracene-1,4,5,8-tetrones. Unusual reactivities with amines.

  The Journal of organic chemistry 20020503