NAMES AND DATABASE IDS
NAMES AND DATABASE IDS
Names Database IDs
IUPAC name
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IUPAC Traditional name
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triphenyltin
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triphenyltin hydride
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Synonyms
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Triphenyltin hydride
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Triphenyltin hydride
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Triphenylstannane
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三苯基锡化氢
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三苯基氢化锡
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CAS Number
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EC Number
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MDL Number
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Beilstein Number
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PubChem SID
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PubChem CID
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CHEBI ID
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Chemspider ID
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Wikipedia Title
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DATA SOURCES
DATA SOURCES
All Sources Commercial Sources Non-commercial Sources
CALCULATED PROPERTIES
CALCULATED PROPERTIES
JChem
H Acceptors
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0
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H Donor
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0
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LogD (pH = 5.5)
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3.9806
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LogD (pH = 7.4)
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3.9806
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Log P
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3.9806
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Molar Refractivity
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77.2229 cm3
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Polarizability
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34.806534 Å3
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Polar Surface Area
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0.0 Å2
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Rotatable Bonds
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3
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Lipinski's Rule of Five
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true
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DETAILS
DETAILS
Wikipedia
Sigma Aldrich
REFERENCES
REFERENCES
From Suppliers
Google Scholar
PubMed
Google 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
PubChem Patent
Google Patent