ChemicalBook--->CAS DataBase List--->17955-46-3

17955-46-3

17955-46-3 Structure

17955-46-3 Structure
IdentificationBack Directory
[Name]

TRIBUTYLSTANNYLTRIMETHYLSILANE
[CAS]

17955-46-3
[Synonyms]

SKL1120
(TRIMETHYLSILYL)TRIBUTYLTIN
TRIMETHYLSILYLTRI-N-BUTYLTIN
TRIBUTYLSTANNYLTRIMETHYLSILANE
Tributyl(trimethylsilyl)stannane
Trimethylsilyltri-n-butyltin 97%
TRIMETHYL(TRIBUTYLSTANNYL)SILANE
(TRIMETHYLSILYL)TRIBUTYLSTANNANE
TRI-n-BUTYLSTANNYLTRIMETHYLSILANE
Stannane, tributyl(trimethylsilyl)-
Trimethyl(tributylstannyl)silane 97%
(Tributylstannyl)trimethylsilane 97%
TRIBUTYLSTANNYLTRIMETHYLSILANE ISO 9001:2015 REACH
(Trimethylsilyl)tri-n-butyltin, Tributyl(trimethylsilyl)stannane
(Tributylstannyl)trimethylsilane, (Trimethylsilyl)tributylstannane, (Trimethylsilyl)tributyltin
(Tributylstannyl)trimethylsilane, (Trimethylsilyl)tributylstannane, (Trimethylsilyl)tributyltin, Tributyl(trimethylsilyl)stannane
[Molecular Formula]

C15H36SiSn
[MDL Number]

MFCD00054903
[MOL File]

17955-46-3.mol
[Molecular Weight]

363.24
Chemical PropertiesBack Directory
[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.
[Specific Gravity]

1.040
[Hydrolytic Sensitivity]

1: no significant reaction with aqueous systems
[BRN ]

4127163
Safety DataBack Directory
[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
[F ]

10-21
[TSCA ]

No
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[HS Code ]

29319090
Hazard InformationBack Directory
[Physical properties]

colorless liquid. bp 88 °C (0.2 mmHg).
[Uses]

Trimethylsilyltributylstannane 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.
[Preparation]

By treating freshly distilled tri-n-butylstannane with LDA followed by quenching with chlorotrimethylsilane.
Spectrum DetailBack Directory
[Spectrum Detail]

TRIBUTYLSTANNYLTRIMETHYLSILANE(17955-46-3)1HNMR
TRIBUTYLSTANNYLTRIMETHYLSILANE(17955-46-3)13CNMR
TRIBUTYLSTANNYLTRIMETHYLSILANE(17955-46-3)IR
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