10436-25-6 | Boc-11-aminoundecanoic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$23.00	$16.00
10g	98%	in stock	$46.00	$32.00
25g	98%	in stock	$110.00	$77.00

Description

• Catalog Number: AB71421
• Chemical Name: Boc-11-aminoundecanoic acid
• CAS Number: 10436-25-6
• Molecular Formula: C16H31NO4
• Molecular Weight: 301.4216
• MDL Number: MFCD00076902
• SMILES: OC(=O)CCCCCCCCCCNC(=O)OC(C)(C)C

Computed Properties

• Complexity: 297
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 21
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 13
• XLogP3: 4.2

Upstream Synthesis Route

Boc-11-aminoundecanoic acid, also known as tert-butoxycarbonyl-11-aminoundecanoic acid, is a key intermediate in chemical synthesis due to its versatile applications in peptide and pharmaceutical industries. As a derivative of amino acids, it plays a crucial role in protecting amino functionalities during peptide synthesis. The Boc (tert-butoxycarbonyl) group serves as a protective group, shielding the amino group from unwanted reactions, allowing for selective modifications at other sites on the peptide chain.In peptide synthesis, Boc-11-aminoundecanoic acid acts as a building block for the construction of peptide chains by selectively deprotecting the Boc group when needed to expose the amino group for further coupling reactions. This controlled deprotection step ensures the sequential assembly of amino acids to form complex peptide structures with high purity and yield.Furthermore, Boc-11-aminoundecanoic acid offers flexibility in peptide design and modification, allowing chemists to incorporate specific amino acids in desired sequences to create custom peptides with tailored properties. Its compatibility with various peptide coupling reagents and solid-phase synthesis techniques makes it a valuable tool for the creation of peptide libraries, bioconjugates, and peptide-based therapeutics.Overall, Boc-11-aminoundecanoic acid plays a pivotal role in chemical synthesis by facilitating the precise construction of peptide molecules essential for drug discovery, biomedical research, and therapeutic applications.