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Chemical substance record

Felbamate

25451-15-4C11H14N2O4238.243 g/mol

The bis(carbamate ester) of 2-phenylpropane-1,3-diol. An anticonvulsant, it is used in the treatment of epilepsy. — ChEBI

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Identity & molecular properties

Source-linked values
CAS number25451-15-4ChEBI ↗
Molecular formulaC11H14N2O4ChEBI ↗
Molar mass238.243 g/molChEBI ↗
Monoisotopic mass238.09536 DaChEBI ↗
Formal charge0ChEBI ↗
ChEBI identifierCHEBI:4995ChEBI ↗

Cross-source molecular data

PubChem
Molar mass238.24 g/molPubChem ↗
Exact mass238.09535693 DaPubChem ↗
Computed XLogP0.6PubChem ↗
Topological polar surface area (Ų)105PubChem ↗
H-bond donors2PubChem ↗
H-bond acceptors4PubChem ↗
Rotatable bonds7PubChem ↗

PubChem computed values are shown separately from the ChEBI record. An exact InChIKey match was used to connect the records. Molecular descriptors do not describe a supplied product’s purity, particle size or performance.

Names & structural identifiers

Copy any identifier
felbamate
2-phenylpropane-1,3-diyl dicarbamate
WKGXYQFOCVYPAC-UHFFFAOYSA-N
NC(=O)OCC(COC(N)=O)c1ccccc1
InChI=1S/C11H14N2O4/c12-10(14)16-6-9(7-17-11(13)15)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H2,12,14)(H2,13,15)

Names & synonyms

2-phenylpropane-1,3-diyl dicarbamatefelbamatofelbamatum

Names are supplied by ChEBI. Trade names and related synonyms may describe a broader product context.

Classification & relationships

ChEBI ontology

Roles recorded in ChEBI

antipsychotic agentanticonvulsantneuroprotective agentanti-anaemic agent

Database role annotations describe reported biological or chemical roles; they are not product approvals or recommendations for use.

Mass ↔ amount of substance

Calculated from sourced mass
Equivalent amount
0.0041974 mol

Uses 238.243 g/mol from ChEBI. Assumes the substance described by this record; no purity or concentration correction is applied.

Elemental composition

Theoretical mass fractions
C
Carbon · 11 atoms
55.46%
O
Oxygen · 4 atoms
26.86%
N
Nitrogen · 2 atoms
11.76%
H
Hydrogen · 14 atoms
5.92%

Calculated theoretical mass fractions from the reported formula and PubChem periodic-table atomic masses. These are not assay or purity results.

Research & patent references

Selected source associations
Synthesis and anticonvulsant activity of novel bicyclic acidic amino acids. ↗Journal of medicinal chemistry · 2003 Jul 3 · PMID 12825948
Topological virtual screening: a way to find new anticonvulsant drugs from chemical diversity. ↗Bioorganic & medicinal chemistry letters · 2003 Aug 18 · PMID 12873507
US2884444 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.
US4978680 · Patent reference ↗Patent cross-reference supplied by ChEBI. Association alone does not establish claim scope.

Sources & record history

Checked 27 Sep 2026
EMBL-EBI ChEBI · CHEBI:4995

Release 255, 9 September 2026. ChEBI three-star (manually annotated) source entry. View original record ↗ · CC BY 4.0

NCBI PubChem · CID 3331 · retrieved 2026-09-27

PubCAS formats source data, connects references and computes explicitly labelled conversions. CAS cross-references are supplied by ChEBI; they do not constitute CAS verification or endorsement.