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Aphos Pd G3 35

An aromatic amine, C27H37N2O3PPdS, 607.065 g/mol. Appears in 96 documented reactions across 8 classes.

Organic — aromatic amine, 96 documented reactions

Identifiers

Molecular formula
C₂₇H₃₇N₂O₃PPdS
Molecular weight
607.065 g/mol
Exact mass
606.129737 g/mol
SMILES
CC(C)(C)P(c1ccc(N)cc1)(C(C)(C)C)->[Pd]1(<-Nc2ccccc2-c2ccccc21)OS(C)(=O)=O
InChI
Not recorded
InChIKey
Not recorded

Calculated properties

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

logP
5.5078calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
86.49 Ųcalculated · chemistry engine
Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors
2calculated · chemistry engine
Atoms that can donate a hydrogen bond.
H-bond acceptors
5calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
6calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
148.7676 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.3333calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.2202calculated · 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
35
Total atoms, hydrogen included
72
Rings
3
Aromatic rings
3
Stereocentres
1
Formal charge
0

Functional groups

  • Primary aromatic amine

    An –NH2 group attached directly to an aromatic ring, as in aniline. Much less basic than an alkyl amine, because the lone pair is delocalised into the ring.

  • 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

96 documented reactions involve Aphos Pd G3 35, each with a written procedure and a source across 8 classes. A few from each are shown.

Buchwald–Hartwig amination

Buchwald–Hartwig amination · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Suzuki–Miyaura coupling

Suzuki–Miyaura coupling · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Palladium-catalysed enolate arylation

Palladium-catalysed enolate arylation · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Buchwald–Hartwig etherification

Buchwald–Hartwig etherification · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Mizoroki–Heck reaction

Mizoroki–Heck reaction · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Buchwald–Hartwig phosphination

Buchwald–Hartwig phosphination · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Sonogashira coupling

Sonogashira coupling · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Buchwald–Hartwig thioetherification

Buchwald–Hartwig thioetherification · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

Buchwald–Hartwig amination

Buchwald–Hartwig amination · as a reagent

A recorded experiment with its conditions, its yield where one was published, and a link to the source.

All 5 buchwald–hartwig amination recordsAll 5 suzuki–miyaura coupling recordsAll 5 palladium-catalysed enolate arylation recordsAll 5 buchwald–hartwig etherification recordsAll 5 mizoroki–heck reaction recordsAll 5 buchwald–hartwig phosphination recordsAll 5 sonogashira coupling recordsAll 5 buchwald–hartwig thioetherification records

Structurally related

Nothing structurally close to Aphos Pd G3 35 has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Aphos Pd G3 35. 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

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.