Details
Quality Factory Hot Selling Hexamethyldistannane 661-69-8 with Fast Shipping
- Molecular Formula: C6H18 Sn2
- Molecular Weight: 327.629
- Appearance/Colour: Clear colorless liquid
- Vapor Pressure: 1.35mmHg at 25°C
- Melting Point: 23-24 ºC
- Refractive Index: n20/D 1.540
- Boiling Point: 182 ºC (756 mmHg)
- Flash Point: 62 ºC
- PSA: 0.00000
- Density: 1.58
- LogP: 2.74120
Hexamethyldistannane(Cas 661-69-8) Usage
|
Reference |
Tsuji, Y.; Kakehi, T., PALLADIUM-CATALYZED DIMERIZATION DOUBLE STANNATION OF 1,3-DIENES USING HEXAMETHYLDISTANNANE. J. Chem. Soc.-Chem. Commun. 1992, 1000-1001. Bumagin, N. A.; Kasatkin, A. N.; Beletskaya, I. P., REACTIONS OF HEXAMETHYLDISTANNANE WITH ALLYL ACETATES AND ALLYL HALIDES CATALYZED BY PALLADIUM COMPLEXES. Bulletin of the Academy of Sciences of the Ussr Division of Chemical Science 1984, 33, 588-594. Benaglia, M.; Toyota, S.; Woods, C. R.; Siegel, J. S., Synthesis of pyridylstannanes from halopyridines and hexamethyldistannane with catalytic palladium. Tetrahedron Lett. 1997, 38, 4737-4740. Mitchell, T. N.; Amamria, A.; Killing, H.; Rutschow, D., SYNTHESIS OF (Z)-1,2-BIS(TRIMETHYLSTANNYL)-1-ALKENES BY PLATINUM-CATALYZED ADDITION OF HEXAMETHYLDISTANNANE TO 1-ALKYNES. J. Organomet. Chem. 1983, 241, C45-C47. |
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Hazard |
A poison by ingestion. |
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Purification Methods |
Wash it with H2O and extract with *C6H6, dry by filtering through powdered Na2SO4, remove *C6H6 on a rotary evaporator and fractionally distil the oily residue under vacuum (b 85-88o/45mm). It boils at ca 182o at atmospheric pressure, but it cannot be distilled in air because the hot vapours flash in the condenser. [Kraus & Session J Am Chem Soc 47 2361 1925, Morris & Selwood J Am Chem Soc 63 2509 1941, Pedley et al. Trans Faraday Soc 53 1612 1957, Beilstein 4 IV 4346.] |
InChI:InChI=1/6CH3.2Sn/h6*1H3;;/rC6H18Sn2/c1-7(2,3)8(4,5)6/h1-6H3
661-69-8 Relevant articles
Magnetic isotope effect in the photolysis of organotin compounds
Buchachenko, Anatoly L.,Ivanov, Vladimir L.,Roznyatovsky, Vitaly A.,Ustynyuk, Yuri A.
, p. 3857 - 3859 (2006)
Photolysis of organotin molecules RSnMe3...
Reaction of α-(trialkylstannyl)acetylenes with metallic sodium
Komarov, N. V.,Andreev, A. A.,Shein, O. G.
, (1994)
α-Trialkylstannylacetylenes react under ...
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Kraus,Neal
, p. 4426,4427,4432 (1930)
-
Chemically induced magnetic isotope effect on the tin nuclei during the photolysis of (1-fluorenyl)trimethyltin
Buchachenko,Roznyatovskii,Ivanov,Ustynyuk
, p. 1009 - 1010 (2006)
A magnetic isotope effect on the 117Sn a...
The palladium-catalysed addition of hexamethylditin to 1,3-dienes
Mitchell, T.N.,Kowall, B.,Killing, H.,Nettelbeck, C.
, p. 101 - 105 (1992)
The addition of the tin-tin bond of hexa...
A simple synthesis of hexamethyldistannane from bis(trimethylstannyl)sulphide
Capozzi, Giuseppe,Menichetti, Stefano,Ricci, Alfredo,Taddei, Maurizio
, p. 285 - 288 (1988)
A new and cheap synthesis of hexamethyld...
Microsolvation, aggregation, and pseudomonomolecular, ionic sp 2-stereoinversion mechanism of two exocyclic β,β-di-tert- alkyl-α-arylvinyllithiums This article is dedicated to Professor Paul Knochel in recognition of his kind support.
Knorr, Rudolf,Hennig, Karsten-Olaf,B?hrer, Petra,Schubert, Bernhard
, p. 125 - 135 (2014/07/08)
A THF-solvated, crystalline, exocyclic a...
Reactions of a Zn(i) complex with group 14 azides-formation of zinc azide and zinc hexazene complexes
Gondzik,Schulz,Blaeser,Woelper,Haack,Jansen
supporting information, p. 927 - 929 (2014/01/06)
Two zinc hexazene complexes L2Zn2(μ-1,6-...
Low-coordinate cobalt fluoride complexes: Synthesis, reactions, and production from C-F activation reactions
Dugan, Thomas R.,Goldberg, Jonathan M.,Brennessel, William W.,Holland, Patrick L.
, p. 1349 - 1360 (2012/04/10)
A cobalt(II) fluoride complex, [LtBuCo(μ...
Synthesis of 1-stannacyclopent-3-enes and their pyrolysis to stannylenes
Zhou, Dong,Reiche, Clemens,Nag, Mrinmoy,Soderquist, John A.,Gaspar, Petet P.
, p. 2595 - 2608 (2009/10/01)
1,1-Diorgano-1-stannacyclopent-3-enes ha...
661-69-8 Process route
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-
1631-73-8
trimethylstannane
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-
1333-74-0
hydrogen
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-
661-69-8
hexamethyldistannane
| Conditions | Yield |
|---|---|
|
trimethylstannyl sodium;
In
not given;
under argon, at 0°C; GLC;
Kinetics;
|
94%
98% |
-
-
1631-73-8
trimethylstannane
-
-
4111-54-0
lithium diisopropyl amide
-
-
1333-74-0
hydrogen
-
-
661-69-8
hexamethyldistannane
| Conditions | Yield |
|---|---|
|
With
O;
In
cyclohexane;
byproducts: i-Pr2NH; LDA (1.88 mmol) in C6H12 placed in Schlenk tube at 0°C under Ar, TMTH (3.76 mmol) added, stirred for 30 min, hydrolysis; Sn2Me6 detected by GC;
|
93%
98% |
|
In
diethyl ether; cyclohexane;
byproducts: i-Pr2NH; TMTH in Et2O cooled to 0°C under Ar, LDA in cyclohexane (1.6 M) added via syringe, stirred for 60 min at room temp., hydrolysis;
|
90%
95% |
|
In
diethyl ether;
byproducts: i-Pr2NH; LDA (1.88 mmol) in C6H12 placed in Schlenk tube at 0°C under Ar, TMTH (3.76 mmol) added, stirred for 30 min, hydrolysis; Sn2Me6 detected by GC;
|
83%
93% |
661-69-8 Upstream products
-
16643-09-7
trimethylstannyl sodium
-
6973-40-6
2,4,6-trinitrophenyl phenyl ether
-
38423-82-4
potassium trimethylstannate
-
17946-71-3
lithium trimethylstannyl
661-69-8 Downstream products
-
4158-75-2
hexa-p-tolyldistannane
-
121848-29-1
1,1,1-trimethyl-2,2,2-tri-p -tolyl distannane
-
7070-08-8
(1R,4R)-1,7,7-Trimethyl-3-phenyl-bicyclo[2.2.1]hept-2-ene
-
7070-09-9
(1R,4R)-1,7,7-trimethyl-2-phenylbicyclo[2.2.1]hept-2-ene
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