(S)-4-Phenyl-3-propionyl-2-oxazolidinone - CAS 184363-66-4
Catalog: |
BB014127 |
Product Name: |
(S)-4-Phenyl-3-propionyl-2-oxazolidinone |
CAS: |
184363-66-4 |
Synonyms: |
(4S)-3-(1-oxopropyl)-4-phenyl-2-oxazolidinone; (4S)-4-phenyl-3-propanoyl-1,3-oxazolidin-2-one |
IUPAC Name: | (4S)-4-phenyl-3-propanoyl-1,3-oxazolidin-2-one |
Description: | (S)-4-Phenyl-3-propionyl-2-oxazolidinone (CAS# 184363-66-4 ) is a useful research chemical. |
Molecular Weight: | 219.24 |
Molecular Formula: | C12H13NO3 |
Canonical SMILES: | CCC(=O)N1C(COC1=O)C2=CC=CC=C2 |
InChI: | InChI=1S/C12H13NO3/c1-2-11(14)13-10(8-16-12(13)15)9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3/t10-/m1/s1 |
InChI Key: | TYZVFKRBBHHHSX-SNVBAGLBSA-N |
Boiling Point: | 393.1 ℃ / 760 mmHg |
Density: | 1.223 g/cm3 |
MDL: | MFCD06658223 |
LogP: | 2.05440 |
Precautionary Statement: | P261 - P305+P351+P338 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
US-10611739-B2 | Process for preparation of lactone derivatives and intermediates thereof | 20160816 |
US-2019210981-A1 | Process for preparation of lactone derivatives and intermediates thereof | 20160816 |
KR-101118145-B1 | Method for preparing synthetic intermediates of penem or carbapenem antibiotics | 20080904 |
KR-20100028218-A | Method for preparing synthetic intermediates of penem or carbapenem antibiotics | 20080904 |
US-2010125059-A1 | 1-biarylazetidinone derivative | 20070306 |
Complexity: | 284 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 219.08954328 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 219.08954328 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 46.6 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.7 |
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