20587-61-5

Basic information

• Product Name: 2-(2-hydroxyethoxy)ethyl benzoate
• Synonyms: 2-(2-hydroxyethoxy)ethyl benzoate;Ethanol, 2-2-(benzoyloxy)ethoxy-;Diethylene glycol monobenzoate;2-[2-(benzoyloxy)ethoxy]-Ethanol;Benzoic acid 2-(2-hydroxyethoxy)ethyl ester;Benzoic acid 5-hydroxy-3-oxapentane-1-yl ester;Ai3-13034;Diethylene glycol benzoate
• CAS NO: 20587-61-5
• Molecular Formula: C₁₁H₁₄O₄
• Molecular Weight: 210.22646
• EINECS: 243-895-5
• Mol File: 20587-61-5.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 316.2°C at 760 mmHg
• Flash Point: 118.8°C
• Appearance: /
• Density: 1.163g/cm³
• Vapor Pressure: 0.000176mmHg at 25°C
• Refractive Index: 1.523
• PKA: 14.34±0.10(Predicted)
• CAS DataBase Reference: 2-(2-hydroxyethoxy)ethyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-hydroxyethoxy)ethyl benzoate(20587-61-5)
• EPA Substance Registry System: 2-(2-hydroxyethoxy)ethyl benzoate(20587-61-5)

Safety Data

• Hazardous Substances Data: 20587-61-5(Hazardous Substances Data)

Usage

Uses

2-?(2-?Hydroxyethoxy)?ethyl Benzoate is a degradation product of dibenzoate plasticizers

InChI:InChI=1/C11H14O4/c12-6-7-14-8-9-15-11(13)10-4-2-1-3-5-10/h1-5,12H,6-9H2

Upstream product

• 107-21-1 ethylene glycol 
• 65-85-0 benzoic acid 
• 501-65-5 diphenyl acetylene 
• 111-46-6 diethylene glycol 
• 929-06-6 2-(2-Aminoethoxy)ethanol 
• 100-52-7 benzaldehyde 
• 93-97-0 benzoic acid anhydride 
• 90433-74-2 4-benzoyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ethyl ester 
• 98-88-4 benzoyl chloride 

Downstream Products

• 59863-47-7 2-Benzoyloxyethoxyethyl p-toluoate 
• 1192068-71-5 (S)-2-((S)-2-tert-butoxycarbonylaminothiopropionylamino)succinic acid 4-[2-(2-benzoyloxyethoxy)ethyl] ester 1-tert-butyl ester 
• 871026-03-8 2-(2-iodoethoxy)ethyl benzoate 
• 64843-84-1 2-(2-benzoyloxyethoxy)ethoxymethyl chloride 
• 59863-46-6 2-Benzoyloxyethoxyethyl furoate 
• 64050-31-3 1-(2-benzoyloxy-ethoxy)-2-(2-methyl-piperidino)-ethane 
• 93206-11-2 <2-(benzoyloxy)ethoxy>acetic acid, 2-(3-amino-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl)hydrazide 
• 93206-06-5 2-<<<(3-amino-4,5-dihydro-5-oxo-1,2,4-triazin-6-yl)methylamino>carbonyl>methoxy>ethanol benzoate 
• 93206-13-4 2-<(6-amino-7,8-dihydro-8-oxo-1,2,4-triazolo<3,4-f>-1,2,4-triazin-3-yl)methoxy>ethanol benzoate 
• 93206-07-6 2-<(2-amino-3,4-dihydro-4-oxoimidazo<5,1-f>-1,2,4-triazin-7-yl)methoxy>ethanol benzoate 
• 125867-97-2 Succinic acid 3-{3-[2-(2-benzoyloxy-ethoxy)-ethoxycarbonyl]-propionyloxy}-2-bromo-2-nitro-propyl ester 2-(2-benzoyloxy-ethoxy)-ethyl ester 
• 125867-96-1 Succinic acid 2-(2-benzoyloxy-ethoxy)-ethyl ester 2-bromo-3-hydroxy-2-nitro-propyl ester 
• 851961-87-0 benzoic acid 2-(2-bromo-ethoxy)-ethyl ester 
• 93206-05-4 <2-(benzoyloxy)ethoxy>acetic acid 

Relevant articles and documents

Electrochemical esterification reaction of alkynes with diols: Via cleavage of carbon-carbon triple bonds without catalyst and oxidant

A novel electrochemical esterification of alkynes for the synthesis of esters was developed in which diols and their derivatives were used as the partners. This method is green as it is catalyst-free, oxidant-free, and additive-free and shows atom-economy. This is the first example of an electrochemical reaction via cleavage of carbon-carbon triple bonds. Meanwhile, this is also the first example of a carbon-carbon triple bond cleavage reaction of alkynes with diols. This journal is

METHOD FOR PREPARING BENZOIC ACID ESTERS

The invention relates to the method of preparing benzoic acid esters which provides high selectivity of the process, and high yield of the desired product, as well as the reduction of the duration of the esterification process, comprising esterification of benzoic acid with monohydric alcohols having a number of carbon atoms from 6 to 12, or polyhydric alcohols having a number of carbon atoms from 2 to 10, in the presence of metal containing catalyst in the media of aromatic solvent at the stepwise buildup of the temperature of the process to 180-200°C, further to 200-220°C, and then to 240-250°C.