What is the Ethyl trimethylacetate?

Ethyl trimethylacetate is clear colorless liquid, while it's Molecular Formula is C7H14O2. clear colorless liquid Used in Chemical Synthesis: Ethyl trimethylacetate is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity and ability to undergo condensation reactions make it a valuable component in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Used in Flavor and Fragrance Industry: Ethyl trimethylacetate is used as a flavoring agent for its fruity and ester-like aroma. It is commonly used in the food and beverage industry to impart a pleasant taste and smell to various products. Used in Solvent Applications: Due to its solubility properties, Ethyl trimethylacetate is used as a solvent in various industrial processes. It is particularly useful in the paint, coating, and adhesive industries, where it helps to dissolve and mix other components effectively. Used in Research and Development: Ethyl trimethylacetate is used as a research compound in academic and industrial laboratories. Its unique chemical properties and reactivity make it an interesting subject for studying various chemical reactions and mechanisms.

What is the CAS number for Ethyl trimethylacetate?

The CAS number of Ethyl trimethylacetate is 3938-95-2.

What is Ethyl trimethylacetate (3938-95-2) used for?

Ethyl trimethylacetate is a clear colorless liquid that undergoes condensation with acetophenone catalyzed by phosphazene base to yield ß-trimethylsilyloxy ester. Its chemical properties have been studied through NCI(F?) and NCI(NH2?) mass spectra.InChI:InChI=1/C7H14O2/c1-5-9-6(8)7(2,3)4/h5H2,1-4H3

What is the Ethyl trimethylacetate?

Ethyl trimethylacetate is clear colorless liquid, while it's Molecular Formula is C7H14O2. clear colorless liquid Used in Chemical Synthesis: Ethyl trimethylacetate is used as a chemical intermediate for the synthesis of various organic compounds. Its reactivity and ability to undergo condensation reactions make it a valuable component in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Used in Flavor and Fragrance Industry: Ethyl trimethylacetate is used as a flavoring agent for its fruity and ester-like aroma. It is commonly used in the food and beverage industry to impart a pleasant taste and smell to various products. Used in Solvent Applications: Due to its solubility properties, Ethyl trimethylacetate is used as a solvent in various industrial processes. It is particularly useful in the paint, coating, and adhesive industries, where it helps to dissolve and mix other components effectively. Used in Research and Development: Ethyl trimethylacetate is used as a research compound in academic and industrial laboratories. Its unique chemical properties and reactivity make it an interesting subject for studying various chemical reactions and mechanisms.

What is the CAS number for Ethyl trimethylacetate?

The CAS number of Ethyl trimethylacetate is 3938-95-2.

What is Ethyl trimethylacetate (3938-95-2) used for?

Ethyl trimethylacetate is a clear colorless liquid that undergoes condensation with acetophenone catalyzed by phosphazene base to yield β-trimethylsilyloxy ester. Its chemical properties have been studied through NCI(F?) and NCI(NH2?) mass spectra.InChI:InChI=1/C7H14O2/c1-5-9-6(8)7(2,3)4/h5H2,1-4H3

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Product classification

Ethyl trimethylacetate

Name: Ethyl trimethylacetate
CAS: 3938-95-2
Purity: 99%

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Details

Reputable factory supply Ethyl trimethylacetate 3938-95-2 in stock with high standard

Molecular Formula: C7H14O2
Molecular Weight: 130.187
Appearance/Colour: clear colorless liquid
Vapor Pressure: 17mmHg at 25°C
Melting Point: -90 °C
Refractive Index: n20/D 1.391(lit.)
Boiling Point: 118 °C at 760 mmHg
Flash Point: 16.1 °C
PSA： 26.30000
Density: 0.881 g/cm³
LogP: 1.59560

Ethyl trimethylacetate(Cas 3938-95-2) Usage

General Description

Ethyl trimethylacetate undergoes condensation with acetophenone catalyzed by phosphazene base to yield β-trimethylsilyloxy ester. NCI(F?) and NCI(NH2?) mass spectra of a series of ethyl trimethylacetates have been studied.

InChI:InChI=1/C7H14O2/c1-5-9-6(8)7(2,3)4/h5H2,1-4H3

3938-95-2 Relevant articles

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Lochmann,L.,Trekoval,J.

, p. 329 - 336 (1975)

Exploring the catalytic activity of Lewis-acidic uranyl complexes in the nucleophilic acyl substitution of acid anhydrides

Takao, Koichiro,Akashi, Shin

, p. 12201 - 12207 (2017/03/08)

The catalytic activities of several uran...

Chemoselective CaO-mediated acylation of alcohols and amines in 2-methyltetrahydrofuran

Pace, Vittorio,Hoyos, Pilar,Alcántara, Andrés R.,Holzer, Wolfgang

, p. 905 - 910 (2013/07/27)

Calcium oxide is proposed as an innocuou...

Double molecular recognition with aminoorganoboron complexes: Selective alcoholysis of β-dicarbonyl derivatives

Oishi, Shunsuke,Saito, Susumu

supporting information; experimental part, p. 5395 - 5399 (2012/06/18)

Double duty: Aminoorganoboron (AOB) comp...

A mild and efficient chemoselective protection of primary alcohols as pivaloyl esters using La(NO3)3·6H2O as a catalyst under solvent-free conditions

Prabhakar,Suryakiran,Venkateswarlu

, p. 732 - 733 (2008/02/09)

Primary alcohols are selectively and eff...

3938-95-2 Process route

: 64-17-5
ethanol

: 201230-82-2
carbon monoxide

: 75-65-0
tert -butyl alcohol

: 637-92-3
Ethyl tert-butyl ether

: 108-64-5
Ethyl isovalerate

: 3938-95-2
2,2-dimethyl-propanoic acid ethyl ester

: 115-11-7,15220-85-6
isobutene

Conditions

Conditions	Yield
With toluene-4-sulfonic acid; bis-triphenylphosphine-palladium(II) chloride; In various solvent(s); at 119.85 ℃; for 12h; under 45003.6 Torr; Further Variations:; Catalysts; Solvents; Temperatures; Product distribution; in ionic liquid;