Glycidyl acrylate

An ester, C6H8O3, 128.127 g/mol. Boiling point 57 °C @ 2 mm Hg, melting point -41.5 °C, as published.

verified recordOrganic — ester6 measured properties

Identifiers

Molecular formula: C₆H₈O₃
Molecular weight: 128.127 g/mol
Exact mass: 128.047344 g/mol
IUPAC name: oxiran-2-ylmethyl prop-2-enoate
SMILES: C=CC(=O)OCC1CO1
InChI: InChI=1S/C6H8O3/c1-2-6(7)9-4-5-3-8-5/h2,5H,1,3-4H2
InChIKey: RPQRDASANLAFCM-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Measured properties

Published measurements, each with its source. Two readings of one property are both shown, in the units each used.

Boiling Point: 135 °F at 2 mmHg (NTP, 1992)measured · CAMEO Chemicals; 57 °C @ 2 mm Hgmeasured · Hazardous Substances Data Bank (HSDB)
Melting Point: Freezing point: -41.5 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Density: 1.1 (NTP, 1992) - Denser than water; will sinkmeasured · CAMEO Chemicals; 1.1074 @ 20 °C/20 °Cmeasured · Hazardous Substances Data Bank (HSDB)
Solubility: 10 to 50 mg/mL at 68.9 °F (NTP, 1992)measured · CAMEO Chemicals; Insoluble in watermeasured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure: 2.97 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases
Flash Point: 141 °F (NTP, 1992)measured · CAMEO Chemicals; 141 °F (61 °C) (open cup)measured · Hazardous Substances Data Bank (HSDB)

Calculated properties

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

Molecular weight: 128.13 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 128.047344113 Dacalculated · reference compound database; Mass of the most common isotopic form.
XLogP3: 0.4calculated · reference compound database; Estimated oil/water partition, computed by reference compound database.
Polar surface area: 38.8 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 130calculated · reference compound database; A rough measure of how intricate the structure is.
H-bond donors: 0calculated · reference compound database
H-bond acceptors: 3calculated · reference compound database
logP: 0.1144calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 38.83 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: 3calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 3calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 30.896 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: 0.3075calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon6 atoms · 56.2% by mass
O Oxygen3 atoms · 37.5% by mass
H Hydrogen8 atoms · 6.3% 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: 9
Total atoms, hydrogen included: 17
Rings: 1
Aromatic rings: 0
Stereocentres: 1
Formal charge: 0

Functional groups

Ester
A carbonyl bonded to an oxygen that links to another carbon.
Ether
An oxygen bridging two carbons.
Alkene
A carbon–carbon double bond.

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 Glycidyl acrylate yet.

Other names for it

The systematic name on this record is oxiran-2-ylmethyl prop-2-enoate.

The sources also call it 2,3-Epoxypropyl acrylate, Glycidyl propenate, oxiran-2-ylmethyl prop-2-enoate, Acrylic acid glycidyl ester, Acrylic acid, 2,3-epoxypropyl ester, 2-Propenoic acid, oxiranylmethyl ester, Methacyclic acid, 2,3-epoxypropyl ester, 1-Propanol, 2,3-epoxy-, acrylate, glycidyl propenoate, Glycidylester kyseliny akrylove, M 581.

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.

(1S,5R)-6,8-dioxabicyclo(3.2.1)octan-4-one

C6H8O3

(Oxiran-2-yl)methyl 2-fluorobenzoate

C10H9FO3

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Glycidyl acrylate. This says nothing about structure: most of them are the bases, solvents, ligands and catalysts the chemistry needed, and they are here because somebody put them in the same flask.

1,1-Propanedithiol

used as a reactant

C₃H₈S₂, 108.231 g/mol.

Where these values came from

reference compound database7836
compound record
chemistry engine
structure perception

compound record.

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.