88950-64-5 | 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$13.00	$9.00
5g	≥97%	in stock	$15.00	$10.00
15g	95%	in stock	$25.00	$18.00
25g	95%	in stock	$34.00	$24.00
50g	95%	in stock	$67.00	$47.00

Description

• Catalog Number: AB43211
• Chemical Name: 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid
• CAS Number: 88950-64-5
• Molecular Formula: C9H15NO4
• Molecular Weight: 201.2197
• MDL Number: MFCD00083257
• SMILES: O=C(NC1(CC1)C(=O)O)OC(C)(C)C

Computed Properties

• Complexity: 263
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• XLogP3: 0.9

Upstream Synthesis Route

1-(Boc-Amino)cyclopropanecarboxylic acid is a versatile compound utilized in chemical synthesis for its unique properties. With a Boc (tert-butoxycarbonyl) protecting group attached to the amino functionality on the cyclopropane ring, this compound serves as a valuable building block in organic synthesis. The Boc protecting group offers stability and enables selective modification of the amino group during various synthetic transformations.This compound finds application in peptide synthesis, where the Boc protecting group can be selectively removed under mild conditions to expose the amino group for further functionalization. Additionally, 1-(Boc-Amino)cyclopropanecarboxylic acid can be employed in the synthesis of diverse bioactive molecules, pharmaceuticals, and agrochemicals due to its ability to participate in a range of chemical reactions such as amidation, esterification, and cross-coupling reactions.Furthermore, the cyclopropane ring in this compound provides a rigid structural motif that can impart unique conformational properties to the target molecules, making it an attractive building block in drug discovery and materials science. The versatility and reactivity of 1-(Boc-Amino)cyclopropanecarboxylic acid make it a valuable tool for chemists seeking to access complex molecular architectures in a controlled and efficient manner.