Mci-186

An aromatic amide, C10H10N2O, 174.203 g/mol. Boiling point 549 °F at 105 mmHg, melting point 261 to 266 °F, as published.

verified recordOrganic — aromatic amide6 measured properties

Identifiers

Molecular formula: C₁₀H₁₀N₂O
Molecular weight: 174.203 g/mol
Exact mass: 174.079313 g/mol
IUPAC name: 5-methyl-2-phenyl-4H-pyrazol-3-one
SMILES: CC1=NN(c2ccccc2)C(=O)C1
InChI: InChI=1S/C10H10N2O/c1-8-7-10(13)12(11-8)9-5-3-2-4-6-9/h2-6H,7H2,1H3
InChIKey: QELUYTUMUWHWMC-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: 549 °F at 105 mmHg (NTP, 1992)measured · CAMEO Chemicals; 287measured · DrugBank
Melting Point: 261 to 266 °F (NTP, 1992)measured · CAMEO Chemicals; 129.7measured · DrugBank
Solubility: less than 1 mg/mL at 73 °F (NTP, 1992)measured · CAMEO Chemicals; SOL IN HOT WATER & HOT ALCOHOL; SLIGHTLY SOL IN BENZENE; INSOL IN PETROLEUM ETHERmeasured · Hazardous Substances Data Bank (HSDB)
Vapor Pressure: less than 0.01 mmHg at 68 °F (NTP, 1992)measured · CAMEO Chemicals; LESS THAN 0.01 MM @ 20 °Cmeasured · Hazardous Substances Data Bank (HSDB)
LogP: 1.12measured · DrugBank; 1.44measured · SangsterLogP
Refractive Index: MAX ABSORPTION (ALCOHOL): 280 NM SHOULDER (LOG E= 3.6) INDEX OF REFRACTION: 1.637; MAX ABSORPTION (ALCOHOL): 245 NM (LOG E= 1.1)measured · Weast, R.C. (ed.). Handbook of Chemistry and Physics. 60th ed. Boca Raton, Florida: CRC Press Inc., 1979., p. C-471

Calculated properties

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

Molecular weight: 174.2 g/molcalculated · reference compound database; Average mass of one molecule, from reference compound database.
Exact mass: 174.079312947 Dacalculated · reference compound database; Mass of the most common isotopic form.
XLogP3: 1.3calculated · reference compound database; Estimated oil/water partition, computed by reference compound database.
Polar surface area: 32.7 Å²calculated · reference compound database; Polar surface area as computed by reference compound database.
Complexity: 241calculated · 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: 1.7992calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 32.67 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: 51.654 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.2calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.6385calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon10 atoms · 68.9% by mass
N Nitrogen2 atoms · 16.1% by mass
O Oxygen1 atom · 9.2% by mass
H Hydrogen10 atoms · 5.8% 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: 13
Total atoms, hydrogen included: 23
Rings: 2
Aromatic rings: 1
Stereocentres: 0
Formal charge: 0

Functional groups

Amide
A carbonyl bonded directly to nitrogen.
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 Mci-186 yet.

Other names for it

The systematic name on this record is 5-methyl-2-phenyl-4H-pyrazol-3-one.

The sources also call it MCI 186, RefChem:57584, edaravone, 3-METHYL-1-PHENYL-2-PYRAZOLIN-5-ONE, Radicut, Norphenazone, 1-Phenyl-3-methyl-5-pyrazolone, Developer Z, Methylphenylpyrazolone, Norantipyrine, C.I. Developer 1.

Structurally related

Nothing structurally close to Mci-186 has a page here yet.

Where these values came from

reference compound database4021
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.