Oxalyl chloride

An organohalide, C2Cl2O2, 126.926 g/mol. Boiling point 63.5 °C @760 [mm Hg], melting point -16 °C, as published.

verified recordOrganic — organohalide4 measured properties

Identifiers

Molecular formula: C₂Cl₂O₂
Molecular weight: 126.926 g/mol
Exact mass: 125.927535 g/mol
IUPAC name: oxalyl dichloride
SMILES: O=C(Cl)C(=O)Cl
InChI: InChI=1S/C2Cl2O2/c3-1(5)2(4)6
InChIKey: CTSLXHKWHWQRSH-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: 63.5 °C @760 [mm Hg]measured · PAC Chemical Database, U.S. Department of Energy
Melting Point: -16 °Cmeasured · PAC Chemical Database, U.S. Department of Energy
Density: 1.4785 @ 20°Cmeasured · PAC Chemical Database, U.S. Department of Energy
Vapor Pressure: 150.0 [mmHg]measured · Haz-Map, Information on Hazardous Chemicals and Occupational Diseases

Calculated properties

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

Molecular weight: 126.92 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 125.9275346 Dacalculated · reference compound database; Mass of the most common isotopic form.
XLogP3: 1.7calculated · reference compound database; Estimated oil/water partition, computed by reference compound database.
Polar surface area: 34.1 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 75calculated · reference compound database; A rough measure of how intricate the structure is.
H-bond donors: 0calculated · reference compound database
H-bond acceptors: 2calculated · reference compound database
logP: 0.5172calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 34.14 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: 1calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 21.72 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.3796calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

Cl Chlorine2 atoms · 55.9% by mass
O Oxygen2 atoms · 25.2% by mass
C Carbon2 atoms · 18.9% 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: 6
Total atoms, hydrogen included: 6
Rings: 0
Aromatic rings: 0
Stereocentres: 0
Formal charge: 0

Functional groups

Halide (C–X)
A halogen atom attached to carbon.

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 Oxalyl chloride yet.

Other names for it

The systematic name on this record is oxalyl dichloride.

The sources also call it Oxalyl dichloride, Ethanedioyl dichloride, Oxalic dichloride, Oxaloyl chloride, Oxalic acid dichloride, Oxalic acid chloride, Ethanedioyl chloride, R4Y96317DW, DTXSID3058822, RefChem:6088, DTXCID0048137.

Structurally related

Nothing structurally close to Oxalyl chloride has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Oxalyl chloride. 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.

1,2-Dichloroethane

used as a reactant

C₂H₄Cl₂, 98.96 g/mol.

(1,1'-Biphenyl)-3-carboxylic acid

used as a reactant

C₁₃H₁₀O₂, 198.221 g/mol.

Where these values came from

reference compound database65578
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.