889949-18-2 | tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$89.00	$62.00
1g	97%	in stock	$145.00	$102.00
5g	97%	in stock	$603.00	$422.00
25g	97%	in stock	$2,732.00	$1,912.00

Description

• Catalog Number: AB57953
• Chemical Name: tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate
• CAS Number: 889949-18-2
• Molecular Formula: C10H20N2O3
• Molecular Weight: 216.2774
• MDL Number: MFCD04115530
• SMILES: OCC1(N)CCN(C1)C(=O)OC(C)(C)C

Computed Properties

• Complexity: 250
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• Undefined Atom Stereocenter Count: 1
• XLogP3: -0.5

Upstream Synthesis Route

The tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional properties. With its distinct structure containing an amino group, a hydroxymethyl group, and a pyrrolidine ring, this compound serves as a valuable building block in organic synthesis.In chemical synthesis, tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate is commonly employed in the modification and functionalization of various organic molecules. Its amino and hydroxymethyl groups can participate in nucleophilic substitution reactions, facilitating the introduction of different functional groups into a molecule. Additionally, the presence of the pyrrolidine ring imparts conformational rigidity and stereochemical control, making it useful in the synthesis of chiral compounds.Furthermore, tert-Butyl 3-amino-3-(hydroxymethyl)pyrrolidine-1-carboxylate can serve as a protecting group for amines and alcohols during multi-step synthesis, allowing chemists to selectively manipulate specific functional groups without affecting others. This compound's stability and ease of manipulation make it a valuable tool in the construction of complex organic molecules with precise control over stereochemistry and functional group positioning.