26448-91-9

Basic information

• Product Name: ETHYL 4-ETHOXYBUTYRATE
• Synonyms: ethyl 4-ethoxybutanoate
• CAS NO: 26448-91-9
• Molecular Formula: C₈H₁₆O₃
• Molecular Weight: 160.21
• Product Categories: C8 to C9;Carbonyl Compounds;Esters;Building Blocks;C8 to C9;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 26448-91-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 183-186 °C(lit.)
• Flash Point: 160 °F
• Appearance: /
• Density: 0.928 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.341mmHg at 25°C
• Refractive Index: n20/D 1.413(lit.)
• CAS DataBase Reference: ETHYL 4-ETHOXYBUTYRATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL 4-ETHOXYBUTYRATE(26448-91-9)
• EPA Substance Registry System: ETHYL 4-ETHOXYBUTYRATE(26448-91-9)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 26448-91-9(Hazardous Substances Data)

Usage

General Description

Ethyl 4-ethoxybutyrate, also known as ethyl 4-ethoxybutanoate, is an aliphatic ester. Its enthalpy of vaporization at boiling point (457.65K) has been reported to be 39.830kjoule/mol.

InChI:InChI=1/C8H16O3/c1-3-10-7-5-6-8(9)11-4-2/h3-7H2,1-2H3

Upstream product

• 96-48-0 4-butanolide 
• 368-39-8 triethyloxonium fluoroborate 
• 64-17-5 ethanol 
• 123691-74-7 1-ethoxy-3-iodopropane 
• 201230-82-2 carbon monoxide 
• 135679-22-0 3-ethoxypropyl methanesulfonate 
• 7664-93-9 sulfuric acid 
• 52263-97-5 2,2-diethoxytetrahydrofuran 
• 122-51-0 orthoformic acid triethyl ester 
• 42192-16-5 4-Vinyloxy-but-2-ynoic acid ethyl ester 
• 28341-54-0 4-(4-nitrophenoxy)butanoic acid 
• 10374-37-5 4-ethoxybutanoic acid 
• 33563-82-5 4-ethoxy-butyronitrile 
• 42192-14-3 4-Vinyloxy-but-2-ynoic acid 

Downstream Products

• 10374-37-5 4-ethoxybutanoic acid 
• 60905-39-7 butylene glycol monoethyl ether acetate 
• 111-73-9 4-ethoxybutan-1-ol 

Relevant articles and documents

INDOLIZINE DERIVATIVES WHICH ARE APPLICABLE TO NEURODEGENERATIVE DISEASES

The present invention relates to indolizine compounds, and pharmaceutically acceptable compositions thereof, useful as antagonists of P2X7, and for the treatment of P2X7-related disorders.

Orthoester-Dependent Alcoholysis of Lactones. Facile Preparation of 4-Alkoxybutanoates and 5-Alkoxypentanoates

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TRANSITION METAL COMPLEX CATALYZED CARBONYLATION OF ORGANIC HALIDES IN THE PRESENCE OF MOLECULAR SIEVES INSTEAD OF BASE

In the presence of molecular sieves under base free conditions organic halides are successfully carbonylated under carbon monoxide pressure with water or alcohols catalyzed by Co or Pd complex to generate the corresponding carboxylic acids or esters, respectively, in good yields.