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About This Item
Linear Formula:
CH3C(OC2H5)3
CAS Number:
Molecular Weight:
162.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-112-4
Beilstein/REAXYS Number:
506201
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.396 (lit.)
bp
142 °C (lit.)
density
0.885 g/mL at 25 °C (lit.)
SMILES string
CCOC(C)(OCC)OCC
InChI
1S/C8H18O3/c1-5-9-8(4,10-6-2)11-7-3/h5-7H2,1-4H3
InChI key
NDQXKKFRNOPRDW-UHFFFAOYSA-N
Application
Triethyl orthoacetate can be used for the synthesis of:
- Ordered mesoporous carbons for catalysis, electrochemistry and hydrogen storage applications.
- Esters of phosphonic acids, carboxylic acids and phosphinic acids.
- Ethyl alk-4-enoates by Johnson–Claisen rearrangement reaction.
- Benzoxazoles, benzimidazoles and oxazolo[4,5-b]pyridines.
- Quinazolin-4(3H)-one derivatives.
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signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
flash_point_f
102.2 °F - Non-equilibrium method
flash_point_c
39 °C - Non-equilibrium method
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Synthesis of ordered mesoporous carbons with channel structure from an organic-organic nanocomposite
Tanaka S, et al.
Chemical Communications (Cambridge, England), 16, 2125-2127 (2005)
Treatment of Baylis-Hillman adducts with triethyl orthoacetate in the presence of heterogeneous catalysts: a method for the stereoselective synthesis of two different types of trisubstituted alkenes
Das B, et al.
Tetrahedron Letters, 47(43), 7619-7623 (2006)
Silica sulfuric acid catalyzed synthesis of benzoxazoles, benzimidazoles and oxazolo [4, 5-b] pyridines under heterogeneous and solvent-free conditions
Mohammadpoor-Baltork I, et al.
Journal of the Iranian Chemical Society, 5(1), S65-S70 (2008)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| T60402-2L | 04061837638411 |
| T60402-100ML | 04061837353086 |
| T60402-500ML | 04061837353093 |
