Tributylstannane
An organic compound, C12H28Sn, 291.067 g/mol. Boiling point 112.5-113.5 @ 8 mm Hg, density 1.103 @ 20 °C, as published.
Identifiers
- Molecular formula
- C₁₂H₂₈Sn
- Molecular weight
- 291.067 g/mol
- Exact mass
- 292.121296 g/mol
- IUPAC name
- tributylstannane
- CCCC[SnH](CCCC)CCCC
- InChI=1S/3C4H9.Sn.H/c3*1-3-4-2;;/h3*1,3-4H2,2H3;;
- DBGVGMSCBYYSLD-UHFFFAOYSA-N
Measured properties
- Boiling Point
- 112.5-113.5 @ 8 mm Hg
- Density
- 1.103 @ 20 °C
Calculated properties
- Molecular weight
- 291.06 g/mol
- Exact mass
- 292.121303 Da
- Polar surface area
- 0 Ų
- Complexity
- 72
- H-bond donors
- 0
- H-bond acceptors
- 0
- logP
- 4.6138
- Topological polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Rotatable bonds
- 9
- Molar refractivity
- 66.294 cm³/mol
- Fraction sp³ carbons
- 1
- QED drug-likeness
- 0.5439
What it is made of
Elements
Structure
- Heavy atoms, hydrogen excluded
- 13
- Total atoms, hydrogen included
- 41
- Rings
- 0
- Aromatic rings
- 0
- Stereocentres
- 0
- Formal charge
- 0
The molecule in three dimensions
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
Other names for it
The systematic name on this record is tributylstannane.
The sources also call it Tributyltin hydride, Stannane, tributyl-, Tri-n-butyltin, Tributylstannic hydride, Tri-n-butylstannane hydride, DTXSID0040709, CHEBI:27086, TBTC chloride, RefChem:888959, DTXCID8020709, 4XDX163P3D, Tri-n-butyltin hydride.
Structurally related
Seen alongside it in reaction records
Molecules that appear in the same recorded reactions as Tributylstannane. 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.
(E)-4-triethylsilyloxy-4-methyl-1-tri-n-butylstannyl-1-heptene
formed as a product
C₂₆H₅₆OSiSn, 531.53 g/mol.
(RS)-1,1,1-Trifluoro-2-chloro-2-(3,5-difluoro-4-ethoxyphenyl)-3-(3-phenoxybenzyloxy)propane
used as a reactant
C₂₄H₂₀ClF₅O₃, 486.864 g/mol.
1,1-Dimethylethyl 4-[4-(3-amino-2-fluorophenyl)-5-(2-chloro-4-pyrimidinyl)-1,3-thiazol-2-yl]-1-piperidinecarboxylate
formed as a product
C₂₃H₂₅ClFN₅O₂S, 490.004 g/mol.
1,1-Dimethylethyl {1-[4-(3-amino-2-fluorophenyl)-5-(2-chloro-4-pyrimidinyl)-1,3-thiazol-2-yl]-1-methylethyl}carbamate
formed as a product
C₂₁H₂₃ClFN₅O₂S, 463.966 g/mol.
1,1-Dimethylethyl 4-[5-(2-chloro-4-pyrimidinyl)-4-(2-fluoro-3-{[(2-propen-1-yloxy)carbonyl]amino}phenyl)-1,3-thiazol-2-yl]-1-piperidinecarboxylate
used as a reactant
C₂₇H₂₉ClFN₅O₄S, 574.078 g/mol.
Where these values came from
chemistry engine
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.
Where to next
More molecules under T
The rest of this shelf, a hundred names at a time.
Molar mass calculator
Work with C12H28Sn in a calculation, with every element's contribution shown.
Molarity calculator
Grams of Tributylstannane for a volume and a concentration, or the concentration a mass gives.
Open in ReactionLens
The full record in the workstation: every atom, every bond, and the reactions it appears in.