177966-60-8 | Fmoc-L-3-benzothienylalanine

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$11.00	$8.00
250mg	97%	in stock	$13.00	$9.00
1g	97%	in stock	$26.00	$18.00
5g	97%	in stock	$116.00	$82.00
25g	97%	in stock	$519.00	$363.00

Description

• Catalog Number: AB00469
• Chemical Name: Fmoc-L-3-benzothienylalanine
• CAS Number: 177966-60-8
• Molecular Formula: C26H21NO4S
• Molecular Weight: 443.5142
• MDL Number: MFCD00672562
• SMILES: O=C(N[C@H](C(=O)O)Cc1csc2c1cccc2)OCC1c2ccccc2c2c1cccc2

Computed Properties

• Complexity: 665
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 32
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 7
• XLogP3: 5.7

Upstream Synthesis Route

Fmoc-3-Ala(3-benzothienyl)-OH is a critical component in chemical synthesis, especially in the field of peptide chemistry. This compound acts as a versatile building block for the synthesis of peptides due to its unique properties and reactivity. By utilizing Fmoc-3-Ala(3-benzothienyl)-OH in peptide synthesis, chemists can incorporate the amino acid alanine with a 3-benzothienyl protecting group into their peptide sequences efficiently.Through a series of coupling reactions, deprotection steps, and purification processes, Fmoc-3-Ala(3-benzothienyl)-OH enables the controlled and precise construction of peptides with tailored sequences and structures. This compound serves as a key intermediate in the production of peptide-based pharmaceuticals, bioactive peptides, and peptide probes utilized in biological research and drug discovery.In addition to its utility in peptide synthesis, Fmoc-3-Ala(3-benzothienyl)-OH offers chemists the flexibility to introduce specific functional groups and modifications into peptide chains, expanding the scope of potential applications in diverse fields such as biotechnology, materials science, and medicinal chemistry. With its strategic role in peptide assembly, this compound plays a crucial role in advancing the development of novel peptides with enhanced properties and functionalities.