117049-14-6 | Boc-L-phenylglycinol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$6.00	$4.00
5g	97%	in stock	$7.00	$5.00
10g	97%	in stock	$10.00	$7.00
25g	97%	in stock	$15.00	$11.00
100g	97%	in stock	$58.00	$41.00
500g	97%	in stock	$286.00	$201.00

Description

• Catalog Number: AA17460
• Chemical Name: Boc-L-phenylglycinol
• CAS Number: 117049-14-6
• Molecular Formula: C13H19NO3
• Molecular Weight: 237.2949
• MDL Number: MFCD00274206
• SMILES: OC[C@H](c1ccccc1)NC(=O)OC(C)(C)C

Computed Properties

• Complexity: 242
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 17
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 1.8

Upstream Synthesis Route

The (S)-tert-Butyl (2-hydroxy-1-phenylethyl)carbamate is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique structure allows for precise control over the stereochemistry of synthesized molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and other fine chemicals. By incorporating this compound into synthesis routes, chemists can introduce chirality in a controlled manner, leading to the creation of enantiopure products with enhanced biological activity and selectivity. Additionally, the (S)-tert-Butyl (2-hydroxy-1-phenylethyl)carbamate serves as a key intermediate in the preparation of complex organic molecules, enabling efficient and sustainable synthesis strategies in the field of medicinal chemistry and drug discovery.

Literature

• Antithrombotic effects of S 18886, a novel orally active thromboxane A2 receptor antagonist.

  Journal of thrombosis and haemostasis : JTH 20040301

• Synthesis and biological evaluation of new tetrahydronaphthalene derivatives as thromboxane receptor antagonists.

  Bioorganic & medicinal chemistry letters 19980602