(R)-4-Benzyl-2-oxazolidinone CAS 102029-44-7

Introduction:Basic information about (R)-4-Benzyl-2-oxazolidinone CAS 102029-44-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(R)-4-Benzyl-2-oxazolidinone Basic information

Product Name:(R)-4-Benzyl-2-oxazolidinone
Synonyms:4-benzyl-2-0xazolidinone;(R)-4-BENZYL-2-OXAZOLIDINONE HPLC 99+%;(R)-4-BENZYL-2-OXAZOLIDINONE 98.0%;(4R)-4-(Phenylmethyl)-1,3-oxazolidin-2-one;(4R)-4-(Phenylmethyl)-2-oxazolidinone;(4R)-Benzyloxazolidin-2-one;(4R)-Phenylmethyl-2-oxazolidinone;(R)-(+)-4-BENZYL-2-OXAZOLIDINONE FOR SYN
CAS:102029-44-7
MF:C10H11NO2
MW:177.2
EINECS:600-264-2
Product Categories:Asymmetric Synthesis;Chiral Auxiliaries;Peptide;Aromatics;Chiral Reagents;Heterocycles;Ketone;Asymmetric Synthesis;Chiral Building Blocks;Glycidyl Compounds, etc. (Chiral);Synthetic Organic Chemistry;Chiral chemicals;chiral;Chiral Compounds;Oxazolidinone;Oxazolidinone Derivatives
Mol File:102029-44-7.mol

(R)-4-Benzyl-2-oxazolidinone Chemical Properties

Melting point 88-90 °C
alpha 62 º (C=1, CHCl3)
Boiling point 309.12°C (rough estimate)
density 1.1607 (rough estimate)
refractive index 14.5 ° (C=5, MeOH)
storage temp. Inert atmosphere,Room Temperature
solubility Chloroform (Slightly)
pka12.78±0.40(Predicted)
form Crystalline Powder
color White to almost white
Optical Rotation[α]18/D +64°, c = 1 in chloroform
Water Solubility Insoluble in water. Soluble in Chloroform.
Sensitive Hygroscopic
BRN 4782551
InChI1S/C10H11NO2/c12-10-11-9(7-13-10)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,12)/t9-/m1/s1
InChIKeyOJOFMLDBXPDXLQ-SECBINFHSA-N
SMILESO=C1N[C@@H](CO1)Cc2ccccc2
CAS DataBase Reference102029-44-7(CAS DataBase Reference)

Safety Information

Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
3-10
HS Code 29349990
Storage Class11 - Combustible Solids

(R)-4-Benzyl-2-oxazolidinone Usage And Synthesis

Description(R)-4-Benzyl-2-oxazolidinone is a derivative of oxazolidinone. It can be used in the preparation of enantiopure carbocyclic nucleosides, which act as a HIV protease inhibitor. It can also be used as a chiral auxiliary in the enantioselective synthesis of (2R, 2′S)-erythro-methylphenidate, beta-lactams and alpha-amino acids. Its end product includes asymmetric single isomeric drugs such as antitumor, anesthetic and entipasmodic products.
Chemical Propertieswhite to light yellow crystal powde
Usesintermediate for Aliskiren hemifumarate, Darifenacin HBr, Zolmitriptan
Uses(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.
Referenceshttp://www.sigmaaldrich.com/catalog/product/aldrich/300977? lang=en®ion=US
https://www.alfa.com/en/catalog/A16770/ Shieh, Wen Chung, et al. "Synthesis of enantiomerically enriched 4- piperidinylglycine." US, US 6670477B2. 2003.

(R)-4-Benzyl-2-oxazolidinone Preparation Products And Raw materials

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