230197
Triethylsilane
99%
Synonym(s):
NSC 93579, Triethylhydrosilane, Triethylsilicon hydride
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About This Item
Linear Formula:
(C2H5)3SiH
CAS Number:
Molecular Weight:
116.28
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-535-3
Beilstein/REAXYS Number:
1098278
MDL number:
Assay:
99%
Form:
liquid
Quality Level
assay
99%
form
liquid
reaction suitability
reagent type: reductant
refractive index
n20/D 1.412 (lit.)
bp
107-108 °C (lit.)
density
0.728 g/mL at 25 °C (lit.)
SMILES string
CC[SiH](CC)CC
InChI
1S/C6H16Si/c1-4-7(5-2)6-3/h7H,4-6H2,1-3H3
InChI key
AQRLNPVMDITEJU-UHFFFAOYSA-N
Application
Catalyst for:
Catalyst reactivation after catalyst polymerization of styrene
Studies involving the prediction of organosilicon flash points
- Synthesis of a spiro-oxindole blocker of Nav1.7 for the treatment of pain
- Redox initiated cationic polymerization
- Beckmann rearrangement of cyclododecanone oxime
- Regioselective reductive coupling of enones and allenes
Catalyst reactivation after catalyst polymerization of styrene
Studies involving the prediction of organosilicon flash points
Used in a study of the reduction of 2-chromanols; syn-selectivity observed with TES.
Versatile reducing agent
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signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
21.2 °F
flash_point_c
-6 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Kelin Li et al.
Organic letters, 8(21), 4711-4714 (2006-10-06)
[reaction: see text] Reduction of C5-substituted 2-hydroxychromans selectively provides 2,4-cis-chromans using large silane reductants and 2,4-trans-chromans using the smaller silane PhSiH(3). The stereochemical outcome has been rationalized on the basis of a Curtin-Hammett kinetic situation arising from hydride delivery to
Zaihui Zhang et al.
Journal of medicinal chemistry, 56(2), 568-583 (2012-12-19)
Stearoyl-CoA desaturase-1 (SCD1) catalyzes de novo synthesis of monounsaturated fatty acids from saturated fatty acids. Studies have demonstrated that rodents lacking a functional SCD1 gene have an improved metabolic profile, including reduced weight gain, lower triglycerides, and improved insulin response.
Sultan Chowdhury et al.
Bioorganic & medicinal chemistry letters, 21(12), 3676-3681 (2011-05-17)
Starting from the oxindole 2a identified through a high-throughput screening campaign, a series of Na(V)1.7 blockers were developed. Following the elimination of undesirable structural features, preliminary optimization of the oxindole C-3 and N-1 substituents afforded the simplified analogue 9b, which
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 230197-25G | 04061838782434 |
| 230197-100G | 04061838782427 |
| 230197-500G | 04061833498781 |
| 230197-5G | 04061838782441 |