Hexamethyldistannane

  • Name: Hexamethyldistannane
  • CAS: 661-69-8
  • Purity: 99%
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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.

Hazard

A poison by ingestion.

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

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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 ...

-

Kraus,Neal

, p. 4426,4427,4432 (1930)

-

Chemically induced magnetic isotope effect on the tin nuclei during the photolysis of (1-fluorenyl)trimethyltin

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, 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

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, 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.

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Two zinc hexazene complexes L2Zn2(μ-1,6-...

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, p. 1349 - 1360 (2012/04/10)

A cobalt(II) fluoride complex, [LtBuCo(μ...

Synthesis of 1-stannacyclopent-3-enes and their pyrolysis to stannylenes

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, p. 2595 - 2608 (2009/10/01)

1,1-Diorgano-1-stannacyclopent-3-enes ha...

661-69-8 Process route

trimethylstannane
1631-73-8

trimethylstannane

hydrogen
1333-74-0

hydrogen

hexamethyldistannane
661-69-8

hexamethyldistannane

Conditions
Conditions Yield
trimethylstannyl sodium; In not given; under argon, at 0°C; GLC; Kinetics;
94%
98%
trimethylstannane
1631-73-8

trimethylstannane

lithium diisopropyl amide
4111-54-0

lithium diisopropyl amide

hydrogen
1333-74-0

hydrogen

hexamethyldistannane
661-69-8

hexamethyldistannane

Conditions
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%

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