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Tributylstannyltrimethylsilane

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Tributylstannyltrimethylsilane manufacturers

Tributylstannyltrimethylsilane Basic information
Product Name:Tributylstannyltrimethylsilane
Synonyms:Trimethyl(tributylstannyl)silane 97%;Tributyl(trimethylsilyl)stannane;Trimethylsilyltri-n-butyltin 97%;(TRIMETHYLSILYL)TRIBUTYLSTANNANE;(TRIMETHYLSILYL)TRIBUTYLTIN;TRIMETHYLSILYLTRI-N-BUTYLTIN;(Trimethylsilyl)tri-n-butyltin, Tributyl(trimethylsilyl)stannane;(Tributylstannyl)trimethylsilane, (Trimethylsilyl)tributylstannane, (Trimethylsilyl)tributyltin, Tributyl(trimethylsilyl)stannane
CAS:17955-46-3
MF:C15H36SiSn
MW:363.24
EINECS:
Product Categories:Chemical Synthesis;Organometallic Reagents;Organotin;Organotins
Mol File:17955-46-3.mol
Tributylstannyltrimethylsilane Structure
Tributylstannyltrimethylsilane Chemical Properties
Boiling point 102-103 °C0.5 mm Hg(lit.)
density 1.04 g/mL at 25 °C(lit.)
refractive index n20/D 1.488(lit.)
Fp >230 °F
storage temp. Store under Argon
solubility soluble in THF, ether, CH2Cl2, MeOH, hexane, insoluble in water.
form liquid
Specific Gravity1.040
AppearanceColorless to light yellow Liquid
Hydrolytic Sensitivity1: no significant reaction with aqueous systems
BRN 4127163
InChI1S/3C4H9.C3H9Si.Sn/c3*1-3-4-2;1-4(2)3;/h3*1,3-4H2,2H3;1-3H3;
InChIKeyMZUUBYSIDDKUKE-UHFFFAOYSA-N
SMILESCCCC[Sn](CCCC)(CCCC)[Si](C)(C)C
Safety Information
Hazard Codes T,N
Risk Statements 21-25-36/38-48/23/25-50/53
Safety Statements 35-36/37/39-45-60-61
RIDADR UN 2788 6.1/PG 3
WGK Germany 3
10-21
TSCA No
HazardClass 6.1(b)
PackingGroup III
HS Code 29319090
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Acute Tox. 4 Dermal
Aquatic Acute 1
Aquatic Chronic 1
Eye Irrit. 2
Repr. 1B
Skin Irrit. 2
STOT RE 1
MSDS Information
ProviderLanguage
SigmaAldrich English
Tributylstannyltrimethylsilane Usage And Synthesis
Physical propertiescolorless liquid. bp 88 °C (0.2 mmHg).
UsesTrimethylsilyltributylstannane is used for the vicinal bis-functionalization of alkynes, dienes, allenes, activated olefins, 1,1-addition to isonitriles, for generation of metal-free aryl and vinyl anions, for generation of benzynes and quinonedimethanes; stereoselective bis-functionalization-cyclization of diynes, eneynes, bis-allenes, alleneynes, and allenealdehydes; silylation of allylic, propargylic derivatives, and aryl bromides; formation of silyl and stannyl cuprates.It takes part in the reactions of Addition to Alkynes, Synthetic Applications of β-Trialkylsilylvinylstannanes, Addition to Isonitriles, Addition to Alkenes and 1,3-Dienes, Addition to Activated Double Bonds, Addition to Allenes, etc.
PreparationBy treating freshly distilled tri-n-butylstannane with LDA followed by quenching with chlorotrimethylsilane.
Tributylstannyltrimethylsilane Preparation Products And Raw materials
Raw materialsTributyltin chloride-->Tributyltin Hydride-->Chlorotrimethylsilane
Preparation Products1-Cyclohexenyloxytrimethylsilane-->Tributylphenyltin-->Hexabutylditin
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