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892-20-6 molecular structure
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triphenylstannane

ChemBase ID: 130027
Molecular Formular: C18H15Sn
Molecular Mass: 350.0127
Monoisotopic Mass: 351.01956948
SMILES and InChIs

SMILES:
[Sn](c1ccccc1)(c1ccccc1)c1ccccc1
Canonical SMILES:
c1ccc(cc1)[Sn](c1ccccc1)c1ccccc1
InChI:
InChI=1S/3C6H5.Sn/c3*1-2-4-6-5-3-1;/h3*1-5H;
InChIKey:
SBXWFLISHPUINY-UHFFFAOYSA-N

Cite this record

CBID:130027 http://www.chembase.cn/molecule-130027.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
triphenylstannane
IUPAC Traditional name
triphenyltin
triphenyltin hydride
Synonyms
Triphenyltin hydride
Triphenyltin hydride
Triphenylstannane
三苯基锡化氢
三苯基氢化锡
CAS Number
892-20-6
EC Number
212-967-8
MDL Number
MFCD00003004
Beilstein Number
3544353
PubChem SID
24854702
162224312
PubChem CID
6460
5357402
CHEBI ID
30537
Chemspider ID
6217
Wikipedia Title
Triphenyltin_hydride

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
H Acceptors H Donor
LogD (pH = 5.5) 3.9806  LogD (pH = 7.4) 3.9806 
Log P 3.9806  Molar Refractivity 77.2229 cm3
Polarizability 34.806534 Å3 Polar Surface Area 0.0 Å2
Rotatable Bonds Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
insoluble in water expand Show data source
soluble in benzene, THF expand Show data source
Apperance
colorless expand Show data source
Melting Point
26-28°C expand Show data source
28 °C expand Show data source
28 °C(lit.) expand Show data source
Boiling Point
156 °C (0.15 mm Hg) expand Show data source
162-168°C/0.5mm expand Show data source
163-165 °C/0.3 mmHg(lit.) expand Show data source
Flash Point
>110°C(230°F) expand Show data source
>230 °F expand Show data source
113 °C expand Show data source
235.4 °F expand Show data source
Density
1.374 expand Show data source
1.374 g/cm3 expand Show data source
1.374 g/mL at 25 °C(lit.) expand Show data source
Refractive Index
1.6370 expand Show data source
n20/D 1.632(lit.) expand Show data source
Storage Warning
Air & Moisture Sensitive expand Show data source
RTECS
WH8882000 expand Show data source
European Hazard Symbols
Nature polluting Nature polluting (N) expand Show data source
Toxic Toxic (T) expand Show data source
UN Number
3077 expand Show data source
UN3146 expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Hazard Class
6.1 expand Show data source
9 expand Show data source
Packing Group
3 expand Show data source
III expand Show data source
Risk Statements
23/24/25-50/53 expand Show data source
R23/24/25 R50/53 expand Show data source
Safety Statements
26-27/28-45-60-61 expand Show data source
26-27-28-45-60-61 expand Show data source
S26 S27 S28 S45 S60 S61 expand Show data source
TSCA Listed
expand Show data source
GHS Pictograms
GHS06 expand Show data source
GHS09 expand Show data source
GHS Signal Word
Danger expand Show data source
Main Hazard
toxic expand Show data source
GHS Hazard statements
H301-H311-H331-H400-H410 expand Show data source
H301-H311-H331-H410 expand Show data source
GHS Precautionary statements
P261-P273-P280-P301 + P310-P311-P501 expand Show data source
P280H-P303+P361+P353-P305+P351+P338-P309-P310-P501A expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges expand Show data source
RID/ADR
UN 3077 9/PG 3 expand Show data source
Storage Temperature
2-8°C expand Show data source
Purity
97% expand Show data source
Linear Formula
(C6H5)3SnH expand Show data source

DETAILS

DETAILS

Wikipedia Wikipedia Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 244775 external link
Packaging
5, 25 g in glass bottle

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • For general reactions of organotin hydrides, see Tri-n-butyltin hydride, A13298.
  • • Reagent for free-radical desulfurization of the thionocarbonates of 1,2-diols to the corresponding methylenedioxy compounds: J. Org. Chem., 62, 1690 (1997).
  • • 2-(Bromomethyl)penicillin V methyl ester undergoes ring-expansion via the methylene radical, to give the corresponding cepham: Tetrahedron, 44, 5953 (1988):
  • • Hydrostannylation of terminal alkynes is conveniently carried out in the presence of triethylboron. Reaction is faster than with tributyl tin hydride and gives higher yields. Stereoselectivity varies from 69-100% (E): Tetrahedron, 45, 923 (1989):
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PATENTS

PATENTS

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INTERNET

INTERNET

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