Triethylsilane , 98% , 617-86-7
Synonym(s):
NSC 93579;Triethylhydrosilane;Triethylsilane;Triethylsilicon hydride
CAS NO.：617-86-7
Empirical Formula: C6H16Si
Molecular Weight: 116.28
MDL number: MFCD00009018
EINECS: 210-535-3
| Pack Size | Price | Stock | Quantity |
| 25ML | RMB31.20 | In Stock |
|
| 100ML | RMB86.40 | In Stock |
|
| 250ml | RMB191.20 | In Stock |
|
| 500ML | RMB359.20 | In Stock |
|
| 2.5L | RMB1739.20 | In Stock |
|
| others | Enquire |
PRODUCT Properties
| Melting point: | -157°C |
| Boiling point: | 107-108 °C (lit.) |
| Density | 0.728 g/mL at 25 °C (lit.) |
| vapor pressure | >1 hPa (20 °C) |
| refractive index | n |
| Flash point: | 25 °F |
| storage temp. | Store below +30°C. |
| solubility | insol H2O; sol hydrocarbons, halocarbons, ethers. |
| form | liquid |
| Specific Gravity | 0.728 |
| color | colorless |
| Water Solubility | Miscible with water. |
| Sensitive | Moisture Sensitive |
| Hydrolytic Sensitivity | 3: reacts with aqueous base |
| BRN | 1098278 |
| Stability: | Stable, but moisture sensitive. Highly flammable. Generates highly flammable gas (hydrogen) in contact with water, acids and bases. |
| LogP | 3.6 at 20℃ |
Description and Uses
Triethylsilane is a useful versatile reductant since it has a active hydride. It can be used for mediated the palladium-catalyzed dehalogenation reaction of alkyl or aryl halides, the reduction of primary, secondary, and tertiary chlorides, bromides, and iodides catalyzed by iridium, as well as efficient reduction of multiple bonds, azides, imines, and nitro groups, as well as benzyl group and allyl group deprotection. It is also specifically for the hydrosilation of olefins to give alkyl silanes. It is also the catalyst for synthesis of a spiro-oxindole blocker of Nav1.7 for the treatment of pain, redox initiated cationic polymerization and Beckmann rearrangement of cyclododecanone oxime as well as regioselective reductive coupling of enones and allenes.
Triethylsilane serves as an exemplar for organosilicon hydride behavior as a mild reducing agent. It is frequently
chosen as a synthetic reagent because of its availability, convenient
physical properties, and economy relative to other organosilicon
hydrides which might otherwise be suitable for effecting specific
chemical transformations.
This reagent is generally used in these reactions: Hydrosilylations, Silane Alcoholysis, Formation of Singlet Oxygen, Reduction of Acyl Derivatives to Aldehydes, Radical Chain Reductions, Ionic Hydrogenations and Reductive Substitutions(The
polar nature of the Si–H bond enables triethylsilane to act as a
hydride donor to electron-deficient centers.), Reductive Etherifications and Acetal Reductions, Ether Cleavages, Reductive Couplings and Cyclizations, Aromatic Silylations, Generation of Other Triethylsilyl Reagents, etc.
Related Reagents: Phenylsilane–cesium fluoride;
tri-n-butylstannane; tricarbonylchloroiridium–diethyl(methyl)
silane–carbon monoxide; triethylsilane–trifluoroacetic acid.
Safety
| Symbol(GHS) |   GHS02,GHS07 |
| Signal word | Danger |
| Hazard statements | H225-H315-H319-H335 |
| Precautionary statements | P210-P233-P240-P241-P303+P361+P353-P305+P351+P338 |
| Hazard Codes | F,Xi |
| Risk Statements | 11-36/37/38-52/53 |
| Safety Statements | 9-16-29-33-37/39-26-61 |
| RIDADR | UN 1993 3/PG 2 |
| WGK Germany | 1 |
| F | 10-21 |
| TSCA | Yes |
| HazardClass | 3 |
| PackingGroup | II |
| HS Code | 29310095 |
