90719-32-7 | (S)-4-Benzyl-2-oxazolidinone

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$6.00	$4.00
10g	98%	in stock	$8.00	$5.00
25g	98%	in stock	$15.00	$10.00
100g	98%	in stock	$33.00	$23.00

Description

• Catalog Number: AB42981
• Chemical Name: (S)-4-Benzyl-2-oxazolidinone
• CAS Number: 90719-32-7
• Molecular Formula: C10H11NO2
• Molecular Weight: 177.1998
• MDL Number: MFCD00064496
• SMILES: O=C1OC[C@@H](N1)Cc1ccccc1

Computed Properties

• Complexity: 187
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1.7

Upstream Synthesis Route

(S)-4-Benzyl-2-oxazolidinone is a versatile compound widely utilized in chemical synthesis as a chiral auxiliary reagent. This compound serves as a useful tool in asymmetric synthesis by facilitating the creation of enantiomerically enriched products. By exploiting the chirality of (S)-4-Benzyl-2-oxazolidinone, chemists can selectively enhance the stereochemical outcomes of various reactions. Its application extends to the synthesis of pharmaceuticals, natural products, and agrochemicals where precise control over stereochemistry is crucial for biological activity and effectiveness. The utilization of (S)-4-Benzyl-2-oxazolidinone in chemical transformations enables the synthesis of complex molecules with high levels of stereochemical purity, making it a valuable asset in the toolkit of synthetic chemists.

Literature

• A biomimetic polyketide-inspired approach to small-molecule ligand discovery.

  Nature chemistry 20120201

• Enantioselective synthesis of N(alpha)-Fmoc protected (2S,3R)-3-phenylpipecolic acid. A constrained phenylalanine analogue suitably protected for solid-phase peptide synthesis.

  The Journal of organic chemistry 20020308