Tributyl(vinyl)tin

Tributyl(vinyl)tin Basic information
Product Name:Tributyl(vinyl)tin
Synonyms:ETHENYLTRIBUTYLSTANNANE;TIN VINYLTRIBUTYL;VINYLTRIBUTYLSTANNANE;TRIBUTYLSTANNYLETHYLENE;TRIBUTYL(VINYL)TIN;Stannane, tributylvinyl-;Tri-n-butylstannylethylene~Tri-n-butyl(vinyl)stannane;Tri-n-butyl(vinyl)tin,96%
CAS:7486-35-3
MF:C14H30Sn
MW:317.1
EINECS:231-291-4
Product Categories:organic tin;Catalyst;Chemical Synthesis;Organometallic Reagents;Organotin;Organotins;Stannanes;monomer;Classes of Metal Compounds;Sn (Tin) Compounds;Typical Metal Compounds
Mol File:7486-35-3.mol
Tributyl(vinyl)tin Structure
Tributyl(vinyl)tin Chemical Properties
Melting point <0°C
Boiling point 104-106 °C/3.5 mmHg (lit.)
density 1.085 g/mL at 25 °C (lit.)
refractive index n20/D 1.478(lit.)
Fp >230 °F
storage temp. Refrigerator
solubility Chloroform (Soluble), Ethyl Acetate (Sparingly)
form liquid
color Colourless
Specific Gravity1.085
Water Solubility Not miscible or difficult to mix in water.
Hydrolytic Sensitivity1: no significant reaction with aqueous systems
BRN 3537662
Exposure limitsACGIH: TWA 0.1 mg/m3; STEL 0.2 mg/m3 (Skin)
NIOSH: IDLH 25 mg/m3; TWA 0.1 mg/m3
Stability:Light sensitive
InChIKeyQIWRFOJWQSSRJZ-UHFFFAOYSA-N
CAS DataBase Reference7486-35-3(CAS DataBase Reference)
NIST Chemistry ReferenceStannane, tributylethenyl-(7486-35-3)
Safety Information
Hazard Codes T,N
Risk Statements 21-25-36/38-48/23/25-50/53-10
Safety Statements 35-36/37/39-45-60-61
RIDADR UN 2788 6.1/PG 3
WGK Germany 3
13
TSCA No
HazardClass 6.1
PackingGroup III
HS Code 29312000
MSDS Information
ProviderLanguage
Vinyltributylstannane English
SigmaAldrich English
ACROS English
ALFA English
Tributyl(vinyl)tin Usage And Synthesis
Chemical Propertiesclear colorless to pale yellow liquid
UsesTributyl(vinyl)tin is used as a reagent in the palladium catalyzed synthesis of allyl and benzyl ethers. Tributyl(vinyl)tin is also a vinyl nucleophile for bromoacetylene and bromoaromatics.
UsesTributyl(vinyl)tin is used as a reagent in the palladium catalyzed synthesis of allyl and benzyl ethers. It is also a vinyl nucleophile for bromoacetylene and bromoaromatics.
Purification MethodsFractionate the stannane under reduced pressure and taking the middle fraction to remove impurities such as (n-Bu)3SnCl. [Seyferth & Stone J Am Chem Soc 79 515 1957, Beilstein 16 III 1279.]
(Trifluoromethyl)trimethylsilane Chloromethyltributylstannane VINYL ESTER RESIN ALLENYLTRIBUTYLTIN 2,6-Dichloro-3-(tributylstannyl)pyridazine 2-METHYLPROPENE-1-TRIBUTYLSTANNANE 3-ISO-PROPOXY-4-TRIBUTYLSTANNYL-1,2-CYCLOBUTENEDIONE TRIBUTYL(PHENYLETHENYL)TIN E-3-(TRIBUTYLSTANNYL)-2-PROPEN-1-AMINE (1-BUTYL-1-METHYL-4-TRIBUTYLSTANNANYL-BUT-3-ENYLOXY)-TRIMETHYL-SILANE Monobutyltin oxide TRI-N-BUTYL(VINYL-D3)TIN 2-(TRIBUTYLSTANNYL)-5,6-DIHYDRO-[1,4]-DIOXIN 2-TRIBUTYLTIN-ALLYL-1-OL CIS-TRI-N-BUTYL(1-PROPENYL)TIN ETHYL-3-(TRI-N-BUTYLTIN)PROPENOATE Z-(1)-ETHOXY-(2)-(TRIBUTYLSTANNYL)ETHYLEN N-(E)-3-TRIBUTYLTINALLYL-1-NAPHTHALENE-D7-METHYLAMINE

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