1,2-Epoxy-3-(2-propylphenoxy)propane

An aromatic ether, C12H16O2, 192.258 g/mol.

Organic — aromatic ether

Identifiers

Molecular formula: C₁₂H₁₆O₂
Molecular weight: 192.258 g/mol
Exact mass: 192.11503 g/mol
IUPAC name: 2-[(2-propylphenoxy)methyl]oxirane
SMILES: CCCc1ccccc1OCC1CO1
InChI: InChI=1S/C12H16O2/c1-2-5-10-6-3-4-7-12(10)14-9-11-8-13-11/h3-4,6-7,11H,2,5,8-9H2,1H3
InChIKey: TWFDUASEWSCMRO-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

logP: 2.4167calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 21.76 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 0calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 2calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 5calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 55.672 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.5calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.6682calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon12 atoms · 75.0% by mass
O Oxygen2 atoms · 16.6% by mass
H Hydrogen16 atoms · 8.4% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 14
Total atoms, hydrogen included: 30
Rings: 2
Aromatic rings: 1
Stereocentres: 1
Formal charge: 0

Functional groups

Ether
An oxygen bridging two carbons.
Aromatic ring
A flat six-membered ring with delocalised electrons.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves 1,2-Epoxy-3-(2-propylphenoxy)propane yet.

Other names for it

The systematic name on this record is 2-[(2-propylphenoxy)methyl]oxirane.

The sources also call it SCHEMBL3691180, SCHEMBL5392031, SCHEMBL8072232, SCHEMBL8369398, SCHEMBL16872528, SCHEMBL30741307, TWFDUASEWSCMRO-UHFFFAOYSA-N, 1,2-epoxy-3-(2-propylphenoxy) propane, DB-104045.

Structurally related

Molecules sharing this formula, or whose fingerprint is at least 40% similar to this one. Similarity is Tanimoto on Morgan fingerprints over this library only — it is a measure of structural overlap, not of how alike they behave.

(+/-)-(7-Isopropyl-2,3-dihydro-1-benzofuran-2-yl)methanol

C12H16O2

((o-Allylphenoxy)methyl)oxirane

C12H14O2

((o-Methoxyphenoxy)methyl)oxirane

C10H12O3

1,2-Epoxy-3-[2-(2-hydroxyethoxy)phenoxy]propane

C11H14O4

Where these values came from

reference compound database12355851
compound record
chemistry engine
structure perception

No matching record was found in the currently indexed sources (reference compound database)..

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.