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4-Methoxybenzoic Acid

C8H8O3, 152.149 g/mol. Its structure, the values that were measured, the values that were calculated, and where each one came from.

Organic — aromatic carboxylic acid5 measured properties

Drawn from the SMILES. It shows how the atoms are connected — not a photograph of a molecule, and not its shape in space.

Identifiers

Molecular formula
C₈H₈O₃
Molecular weight
152.149 g/mol
Exact mass
152.047344 g/mol
SMILES
COc1ccc(C(=O)O)cc1
InChI
InChI=1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)
InChIKey
ZEYHEAKUIGZSGI-UHFFFAOYSA-N

Both are open without an account.

Measured properties

Values somebody obtained from a sample and published. Where two sources report the same property they are both shown, in the units each used — a disagreement between them is information, and averaging it away would be inventing a number neither one gave.

Boiling Point
276.5 °Cmeasured · PhysProp
275-280 °Cmeasured · reference compound database
Melting Point
185 °Cmeasured · PhysProp
185 °Cmeasured · reference compound database
Solubility
530 mg/L (at 37 °C)measured · YALKOWSKY,SH & DANNENFELSER,RM (1992)
0.53 mg/mL at 37 °Cmeasured · reference compound database
soluble in boiling water, organic solventsmeasured · reference compound database
freely soluble (in ethanol)measured · reference compound database
Vapor Pressure
0.0015 [mmHg]measured · reference compound database
LogP
1.96measured · HANSCH,C ET AL. (1995)
1.96measured · HANSCH,C ET AL. (1995)
1.88measured · reference compound database

Calculated properties

Derived from the structure rather than from a sample. These are reproducible and they are not measurements: a calculated partition coefficient and a measured one can differ by a long way, and where both exist they are listed apart on purpose.

logP
1.3934calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
46.53 Ųcalculated · chemistry engine
Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors
1calculated · chemistry engine
Atoms that can donate a hydrogen bond.
H-bond acceptors
2calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
2calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
39.9533 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.125calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.6961calculated · chemistry engine
Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

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

Structure

Heavy atoms, hydrogen excluded
11
Total atoms, hydrogen included
19
Rings
1
Aromatic rings
1
Stereocentres
0
Formal charge
0

Functional groups

  • Carboxylic acid

    A carbon double-bonded to oxygen and bonded to an –OH group; acidic.

  • 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 4-Methoxybenzoic Acid yet.

Other names for it

No systematic name is recorded.

The sources also call it p-Anisic acid, p-Methoxybenzoic acid, Draconic acid, Benzoic acid, 4-methoxy-, 4-Anisic acid, ANISIC ACID, PARA, para-anisic acid, FEMA NO. 3945, ANISIC ACID, P-Methoxy Benzoic Acid, 4-Methoxy benzoic acid, Methoxybenzoic acid.

Structurally related

Nothing structurally close to 4-Methoxybenzoic Acid has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as 4-Methoxybenzoic Acid. 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.

Where these values came from

  • chemistry engine

    structure perception

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

What this page does not claim

The identifiers are what the source record holds, copied rather than recomputed. Measured values are reported as their source gave them, units and all; calculated values are marked as calculated and are not measurements. Where a field is absent the page says so, because a blank cell reads as a zero and a guessed value reads as a fact.

Nothing here is a hazard assessment, a purity statement or advice about handling a sample. A flash point quoted from a safety database is a number somebody published, not a judgement by us about whether this molecule is safe for what you intend.