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13683-41-5

13683-41-5 Structure

13683-41-5 Structure
IdentificationMore
[Name]

(1-BROMOVINYL)TRIMETHYLSILANE
[CAS]

13683-41-5
[Synonyms]

(1-BROMOVINYL)TRIMETHYLSILANE
α-(trimethylsilyl)vinyl bromide
(1-Bromoethenyl)trimethylsilane
Trimethyl(1-bromoethenyl)silane
(1-Bromoethynl) trimethylsilane
α-(trimethylsilyl)vinyl bromide
1-BROMO-1-TRIMETHYLSILYLETHYLENE
1-Bromo-1-(trimethylsilyl)ethene
(1-Bromovinyl)trimethylsilane,97%
(1-BroMovinyl)triMethylsilane 97%
ALPHA-TRIMETHYLSILYLVINYL BROMIDE
(1-Bromovinyl)trimethylsilane >
Silane, (1-bromoethenyl)trimethyl-
1-Bromo-1-trimethylsilylethylene alpha-Trimethylsilylvinyl Bromide
[EINECS(EC#)]

237-195-9
[Molecular Formula]

C5H11BrSi
[MDL Number]

MFCD00014927
[Molecular Weight]

179.13
[MOL File]

13683-41-5.mol
Chemical PropertiesBack Directory
[Appearance]

CLEAR LIGHT YELLOW LIQUID
[Boiling point ]

124 °C745 mm Hg(lit.)
[density ]

1.156 g/mL at 25 °C(lit.)
[vapor density ]

>1 (vs air)
[refractive index ]

n20/D 1.458(lit.)
[Fp ]

49 °F
[storage temp. ]

2-8°C
[solubility ]

completely miscible with THF and Et2O.
[form ]

clear liquid
[color ]

Colorless to Light yellow to Light orange
[Specific Gravity]

1.163
[Hydrolytic Sensitivity]

4: no reaction with water under neutral conditions
[BRN ]

1742258
[InChI]

InChI=1S/C5H11BrSi/c1-5(6)7(2,3)4/h1H2,2-4H3
[InChIKey]

VVDJVCJVVHHCIB-UHFFFAOYSA-N
[SMILES]

[Si](C(Br)=C)(C)(C)C
[CAS DataBase Reference]

13683-41-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

F
[Risk Statements ]

R11:Highly Flammable.
[Safety Statements ]

S16:Keep away from sources of ignition-No smoking .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
[RIDADR ]

UN 1993 3/PG 2
[WGK Germany ]

3
[F ]

8-10-21
[TSCA ]

No
[HS Code ]

2931.90.9010
[HazardClass ]

3.1
[PackingGroup ]

II
Hazard InformationBack Directory
[Chemical Properties]

CLEAR LIGHT YELLOW LIQUID
[Physical properties]

bp 124°C/745 mmHg; d 1.156 g cm?3.
[Uses]

Numerous nucleophiles react with (1-bromovinyl)trimethylsilane in the presence of palladium complexes. The bromine has been substituted by phenylthio,vinyl,and aryl groups. This approach gives reasonable yields of the desired products. However, the substitution reactions sometimes lack regiospecificity. For example, a mixture of regioisomers was obtained in eq 6. Two mechanisms have been proposed for the formation of the β-substituted product. One involves an elimination step to give trimethylsilylacetylene as an intermediate, which then undergoes catalyzed additions with the nucleophile at either the α- or β-positions.The other mechanism involves the formation of a pentacoordinated palladium intermediate, leading to the formation of isomeric products.

[Preparation]

prepared, in good yield, from the reaction of vinyltrimethylsilane with bromine at low temperature followed by dehydrohalogenation in the presence of an amine base.Alternative syntheses and reagents, i.e. (1-bromovinyl)- triphenylsilane and (1-bromovinyl)triethylsilane, are also known.
[General Description]

Tetrakis(triphenylphosphine)palladium(0) catalyzed coupling reactions of (1-bromovinyl)trimethylsilane with organozinc bromides were studied.
Spectrum DetailBack Directory
[Spectrum Detail]

(1-BROMOVINYL)TRIMETHYLSILANE(13683-41-5)1HNMR
(1-BROMOVINYL)TRIMETHYLSILANE(13683-41-5)Raman
(1-BROMOVINYL)TRIMETHYLSILANE(13683-41-5)FT-IR
(1-BROMOVINYL)TRIMETHYLSILANE(13683-41-5)IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

(1-Bromovinyl)trimethylsilane, 97%(13683-41-5)
[Sigma Aldrich]

13683-41-5(sigmaaldrich)
[TCI AMERICA]

(1-Bromovinyl)trimethylsilane,>96.0%(GC)(13683-41-5)
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