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658405

Sigma-Aldrich

(S)-4-(4-Aminobenzyl)-2(1H)-oxazolidinone

97%

Synonym(s):

(4S)-4-[(4-Aminophenyl)methyl]-2-oxazolidinone

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About This Item

Empirical Formula (Hill Notation):
C10H12N2O2
CAS Number:
152305-23-2
Molecular Weight:
192.21
MDL number:
MFCD03411476
UNSPSC Code:
12352005
PubChem Substance ID:
24884353
NACRES:
NA.22

Assay

97%

form

solid

mp

107-111 °C

SMILES string

Nc1ccc(C[C@H]2COC(=O)N2)cc1

InChI

1S/C10H12N2O2/c11-8-3-1-7(2-4-8)5-9-6-14-10(13)12-9/h1-4,9H,5-6,11H2,(H,12,13)/t9-/m0/s1

InChI key

WNAVSKJKDPLWBD-VIFPVBQESA-N

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Application

(S)-4-(4-Aminobenzyl)-2(1H)-oxazolidinone can be used as a starting material in the synthesis of:
  • Oxazolidinone derived 2-azetidinones as metal cation sensors.
  • Serotonin receptor agonist named zolmitriptan.
  • Schiff base derived zinc metal complexes of biological importance.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Novel zinc (II) complexes of heterocyclic ligands as antimicrobial agents: synthesis, characterisation, and antimicrobial studies
Yamgar RS, et al.
Bioinorganic Chemistry and Applications, 2014 (2014)
(S)-4-(4-aminobenzyl)-2-oxazolidinone based 2-azetidinones for antimicrobial application and luminescent sensing of divalent metal cations
Baruah S, et al.
Journal of Heterocyclic Chemistry, 57, 2498?2511-2498?2511 (2020)
Convenient and Industrially Viable Process for Preparation of Zolmitriptan
Neelakandan K, et al.
Journal of Heterocyclic Chemistry, 51(S1), E332-E334 (2014)
D Manikandan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 239, 118484-118484 (2020-05-30)
The experimental geometry (XRD), vibrational (IR and Raman), electronic (UV-visible) and NMR spectra of (S)-4-(4-Amino-benzyl)-oxazolidin-2-one (ABO) have been corroborated with the corresponding first principle calculated values at DFT using hybrid B3LYP exchange correlation functional invoking 6-311++g(d, p) basis set. The

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