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Palladium(2+);tris(2-methylphenyl)phosphane;dichloride

An aromatic compound, C42H42Cl2P2Pd, 786.072 g/mol.

verified record, Organic — aromatic compound

Identifiers

Molecular formula
C₄₂H₄₂Cl₂P₂Pd
Molecular weight
786.072 g/mol
Exact mass
784.117366 g/mol
IUPAC name
palladium(2+);bis(tris(2-methylphenyl)phosphane);dichloride
SMILES
Cc1ccccc1P(c1ccccc1C)c1ccccc1C.Cc1ccccc1P(c1ccccc1C)c1ccccc1C.Cl[Pd]Cl
InChI
InChI=1S/2C21H21P.2ClH.Pd/c2*1-16-10-4-7-13-19(16)22(20-14-8-5-11-17(20)2)21-15-9-6-12-18(21)3;;;/h2*4-15H,1-3H3;2*1H;/q;;;;+2/p-2
InChIKey
OTYPIDNRISCWQY-UHFFFAOYSA-L

Calculated properties

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

Molecular weight
786.1 g/molcalculated · reference compound database
Average mass of one molecule, from reference compound database.
Exact mass
784.11736 Dacalculated · reference compound database
Mass of the most common isotopic form.
Polar surface area
0 Ųcalculated · reference compound database
Polar surface area as computed by reference compound database.
Complexity
286calculated · 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
10.1166calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
0 Ųcalculated · 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
0calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
6calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
210.424 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.1429calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.1166calculated · 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
47
Total atoms, hydrogen included
89
Rings
6
Aromatic rings
6
Stereocentres
0
Formal charge
0

Functional groups

  • 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 Palladium(2+);tris(2-methylphenyl)phosphane;dichloride yet.

Other names for it

The systematic name on this record is palladium(2+);bis(tris(2-methylphenyl)phosphane);dichloride.

The sources also call it C42H42Cl2P2Pd, SCHEMBL105623, AKOS015915766, SY010266, palladium(2+);tris-o-tolylphosphane;dichloride, F549839.

Structurally related

Nothing structurally close to Palladium(2+);tris(2-methylphenyl)phosphane;dichloride has a page here yet.

Where these values came from

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.