106454-69-7 | N-Boc-D-phenylalaninol

Packsize	Purity	Availability	Price	Discounted Price
10g	98%	in stock	$10.00	$7.00
25g	98%	in stock	$19.00	$14.00

Description

• Catalog Number: AD77912
• Chemical Name: N-Boc-D-phenylalaninol
• CAS Number: 106454-69-7
• Molecular Formula: C14H21NO3
• Molecular Weight: 251.3214
• MDL Number: MFCD00216472
• SMILES: OC[C@@H](Cc1ccccc1)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 254
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 18
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 6
• XLogP3: 2.3

Upstream Synthesis Route

Boc-D-Phenylalaninol, also known as N-tert-butoxycarbonyl-D-phenylalaninol, is a key building block in chemical synthesis. Its primary application lies in peptide synthesis, where it serves as a versatile reagent for incorporating D-phenylalanine into peptide chains.In peptide synthesis, Boc-D-Phenylalaninol is commonly used for the selective protection of the hydroxyl group on the amino acid, enabling specific chemical reactions to occur without interfering with other functional groups present in the peptide molecule. This protection strategy allows for controlled and efficient coupling reactions during peptide assembly, leading to high product yields and purity.Furthermore, the Boc (tert-butoxycarbonyl) protecting group can be easily removed under mild acidic conditions, revealing the free hydroxyl group for subsequent manipulation or further reactions. This flexibility in functional group manipulation makes Boc-D-Phenylalaninol a valuable tool in the synthesis of complex peptides and peptidomimetics with precise stereochemistry.Overall, Boc-D-Phenylalaninol plays a crucial role in modern chemical synthesis, particularly in the field of peptide chemistry, where its strategic use enhances the efficiency and control of peptide bond formation.