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(Trimethylsilyl)acetylene, 98%, Thermo Scientific Chemicals
67.94 € - 409.04 €
Chemical Identifiers
| CAS | 1066-54-2 |
|---|---|
| Molecular Formula | C5H10Si |
| Molecular Weight (g/mol) | 98.22 |
| MDL Number | MFCD00008569 |
| InChI Key | CWMFRHBXRUITQE-UHFFFAOYSA-N |
| Synonym | trimethylsilylacetylene, trimethylsilyl acetylene, silane, ethynyltrimethyl, ethynyl-trimethyl-silane, ethynyl trimethyl silane, tms acetylene, ethynyltrimethyl silane, trimethylsilyl-acetylene, tmsacetylene |
| PubChem CID | 66111 |
| IUPAC Name | ethynyl(trimethyl)silane |
| SMILES | C[Si](C)(C)C#C |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11405273
|
Thermo Scientific Alfa Aesar
A12856.06 |
5 g |
67.94 €
5g |
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|
11415273
|
Thermo Scientific Alfa Aesar
A12856.14 |
25 g |
195.98 €
25g |
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|
11425273
|
Thermo Scientific Alfa Aesar
A12856.22 |
100 g |
409.04 €
100g |
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Description
(Trimethylsilyl)acetylene is used in the preparation of trimethylsilanyl-propiolic acid ethyl ester by reacting with carbonochloridic acid ethyl ester as well as in the synthesis of iodoalkenes by radical addition of perfluoroalkyl iodides. It is used as a nucleophile in Friedel-Crafts type acylations and alkylations reactions, as a ligand in organometallic chemistry and an useful reagent in cycloaddition reactions. It acts as a precursor to lithium trimethylsilylacetylide It finds application in the synthesis of (±)-estrone.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications(Trimethylsilyl)acetylene is used in the preparation of trimethylsilanyl-propiolic acid ethyl ester by reacting with carbonochloridic acid ethyl ester as well as in the synthesis of iodoalkenes by radical addition of perfluoroalkyl iodides. It is used as a nucleophile in Friedel-Crafts type acylations and alkylations reactions, as a ligand in organometallic chemistry and an useful reagent in cycloaddition reactions. It acts as a precursor to lithium trimethylsilylacetylide It finds application in the synthesis of (±)-estrone.
Solubility
Miscible with organic solvents.
Notes
Store in a cool place. Incompatible with strong oxidizing agents.
Chemical Identifiers
| 1066-54-2 | |
| 98.22 | |
| CWMFRHBXRUITQE-UHFFFAOYSA-N | |
| 66111 | |
| C[Si](C)(C)C#C |
| C5H10Si | |
| MFCD00008569 | |
| trimethylsilylacetylene, trimethylsilyl acetylene, silane, ethynyltrimethyl, ethynyl-trimethyl-silane, ethynyl trimethyl silane, tms acetylene, ethynyltrimethyl silane, trimethylsilyl-acetylene, tmsacetylene | |
| ethynyl(trimethyl)silane |
Specifications
| 52°C to 53°C | |
| C5H10Si | |
| MFCD00008569 | |
| 906752 | |
| trimethylsilylacetylene, trimethylsilyl acetylene, silane, ethynyltrimethyl, ethynyl-trimethyl-silane, ethynyl trimethyl silane, tms acetylene, ethynyltrimethyl silane, trimethylsilyl-acetylene, tmsacetylene | |
| CWMFRHBXRUITQE-UHFFFAOYSA-N | |
| ethynyl(trimethyl)silane | |
| 66111 | |
| 98% | |
| 0.71 |
| 1066-54-2 | |
| HC≡CSi(CH3)3 | |
| UN1993 | |
| <−34°C (−29°F) | |
| Miscible with organic solvents. | |
| C[Si](C)(C)C#C | |
| 98.22 | |
| 98.22 | |
| 1.39 | |
| (Trimethylsilyl)acetylene |
Safety and Handling
GHS H Statement
H225
Highly flammable liquid and vapour.
P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378q-P501c
H225
missing translation for 'dotInformation' : Transport Hazard Class: 3; Packing Group: II; Proper Shipping Name: FLAMMABLE LIQUIDS, N.O.S.
missing translation for 'einecsNumber' : 213-919-9
missing translation for 'tsca' : Yes
Recommended Storage : Keep cold
RUO – Research Use Only