106391-87-1 | Boc-D-valinol

Packsize	Purity	Availability	Price	Discounted Price
5g	95%	in stock	$19.00	$13.00
25g	95%	in stock	$28.00	$20.00

Description

• Catalog Number: AI06959
• Chemical Name: Boc-D-valinol
• CAS Number: 106391-87-1
• Molecular Formula: C10H21NO3
• Molecular Weight: 203.2786
• MDL Number: MFCD00235960
• SMILES: OC[C@@H](C(C)C)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 184
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 1.6

Upstream Synthesis Route

Boc-D-Valinol, also known as tert-butoxycarbonyl-D-valinol, is a key compound with versatile applications in chemical synthesis. As a derivative of the amino acid valine, Boc-D-Valinol plays a crucial role in the protection of amino groups during peptide synthesis. By utilizing the Boc protecting group, chemists can selectively shield the amino group of valine, preventing undesired reactions and allowing for controlled manipulation of the molecule in peptide assembly.In addition to its use as a protecting group, Boc-D-Valinol is also employed in the asymmetric synthesis of organic compounds. Its chiral nature enables the creation of enantiomerically pure molecules, making it a valuable building block in medicinal chemistry and drug development. The incorporation of Boc-D-Valinol in synthetic routes allows for the efficient and precise construction of complex molecules with defined stereochemistry.Furthermore, Boc-D-Valinol can serve as a catalyst or ligand in various chemical transformations, facilitating the formation of new bonds and accelerating reaction rates. Its versatile reactivity and stability make it a valuable tool for the synthesis of diverse compounds ranging from pharmaceuticals to advanced materials. With its wide-ranging applications in chemical synthesis, Boc-D-Valinol continues to be a vital component in the toolbox of synthetic chemists striving to create novel molecules and advance the frontiers of chemical research.