(R)-(+)-4-Benzyl-2-oxazolidinone, 99%
(R)-(+)-4-Benzyl-2-oxazolidinone, 99%
(R)-(+)-4-Benzyl-2-oxazolidinone, 99%
Thermo Scientific Chemicals

(R)-(+)-4-Benzyl-2-oxazolidinone, 99%

CAS: 102029-44-7 | C10H11NO2 | 177.20 g/mol
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Catalog number A16770.14
also known as A16770-14
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Quantity:
25 g
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Price (USD)
367.65
Online Exclusive
408.00
Save 40.35 (10%)
Each
Chemical Identifiers
CAS102029-44-7
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale cream
Formcrystalline powder
Assay (GC)>98.5%
Water Content (Karl Fischer Titration)<0.5%
Optical Rotation+62.5 ? 3? (c=1 in chloroform)
(R)-(+)-4-Benzyl-2-oxazolidinones are used in the enantioselective synthesis of beta-lactams and alpha-amino acids. End products can include asysmmetric single isomeric drugs of antitumor, anesthetic, antipasmodic products. Used in the synthesis of HIV protease inhibitors. An oxazolidinone used in chiral auxiliary asymetric synthesis.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(R)-(+)-4-Benzyl-2-oxazolidinones are used in the enantioselective synthesis of beta-lactams and alpha-amino acids. End products can include asysmmetric single isomeric drugs of antitumor, anesthetic, antipasmodic products. Used in the synthesis of HIV protease inhibitors. An oxazolidinone used in chiral auxiliary asymetric synthesis.

Solubility
Insoluble in water. Soluble in Chloroform.

Notes
Hygroscopic. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents.
RUO – Research Use Only
David J Madar,; Hana Kopecka,; Daisy Pireh,; Jonathan Pease,; Marina Pliushchev,; Richard J Sciotti,; Paul E Wiedeman,; Stevan W Djuric.Synthesis of N-arylated oxazolidinones via a palladium catalyzed cross coupling reaction. Application to the synthesis of the antibacterial agent Dup-721. Tetrahedron Letters. 2001, 42 (22),3681-3684.