4547-58-4

Basic information

• Product Name: ethyl (4-butoxyphenyl)acetate
• Synonyms: ethyl (4-butoxyphenyl)acetate;4-Butoxybenzeneacetic acid ethyl ester;Einecs 224-905-7
• CAS NO: 4547-58-4
• Molecular Formula: C₁₄H₂₀O₃
• Molecular Weight: 236.3068
• EINECS: 224-905-7
• Mol File: 4547-58-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 322.2°Cat760mmHg
• Flash Point: 132.4°C
• Appearance: /
• Density: 1.017g/cm³
• Vapor Pressure: 0.000283mmHg at 25°C
• Refractive Index: 1.492
• CAS DataBase Reference: ethyl (4-butoxyphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (4-butoxyphenyl)acetate(4547-58-4)
• EPA Substance Registry System: ethyl (4-butoxyphenyl)acetate(4547-58-4)

Safety Data

• Hazardous Substances Data: 4547-58-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H20O3/c1-3-5-10-17-13-8-6-12(7-9-13)11-14(15)16-4-2/h6-9H,3-5,10-11H2,1-2H3

Upstream product

• 64-17-5 ethanol 
• 66786-80-9 1-Butoxy-4-((Z)-2-methanesulfinyl-2-methylsulfanyl-vinyl)-benzene 
• 5736-88-9 p-butoxybenzaldehyde 
• 201230-82-2 carbon monoxide 
• 10519-06-9 1-butoxy-4-methylbenzene 

Downstream Products

• 4547-57-3 4-butoxyphenylacetic acid 
• 15560-35-7 2-(4-Butoxy-phenyl)-propionic acid ethyl ester 
• 15560-38-0 2-(4-Butoxy-phenyl)-2-methyl-propionic acid ethyl ester 
• 15560-23-3 N-Hydroxy-4-butoxy-α-methyl-phenylacetamide 
• 220531-49-7 C₁₄H₁₉BrO₃ 

Relevant articles and documents

PROCESS FOR SYNTHESIZING PHENYLACETIC ACID BY CARBONYLATION OF TOLUENE

A production process for substituted phenylacetic acids or ester analogues thereof is disclosed. In this process toluene or toluene substituted with various substituents, an alcohol, an oxidant and carbon monoxide are used as raw materials to obtain compounds comprising structure of phenylacetic acid ester or analogues thereof by catalysis of the complex catalyst formed from transition metal and ligand, and such compounds are hydrolyzed to obtain various substituted phenylacetic acid based compounds. This type of compounds and their derivatives serve as important fine chemicals used widely in the industries of pharmaceuticals, pesticides, perfume and the like.

Growth hormone secretagogues

What is disclosed are growth hormone secretagogues, and their uses, of the formula wherein R1 is C6H5CH2OCH2—, C6H5(CH2)3— or indol-3-ylmethyl; Y is pyrrolidin-1-yl, 4-C1-C6alkylpiperidin-1-yl or NR2R2; R2 are each independently a C1to C6alkyl; R3 is 2-napthyl or phenyl para-substituted by W; W is H, F, CF3, C1-C6alkoxy or phenyl; and R4 is H or CH3, or a pharmaceutically acceptable salt or solvate thereof.