57981-99-4

Basic information

• Product Name: 2-chloro-1,4-phenylene diacetate
• Synonyms: 2-chloro-1,4-phenylene diacetate;EINECS 261-060-3;CHLOROHYDROQUINONEDIACETATE;2-Chloro-1,4-benzenediol diacetate;Diacetic acid 2-chloro-1,4-phenylene ester;1,4-Benzenediol, 2-chloro-, 1,4-diacetate;1,4-Benzenediol, 2-chloro-, diacetate
• CAS NO: 57981-99-4
• Molecular Formula: C₁₀H₉ClO₄
• Molecular Weight: 228.62906
• EINECS: 261-060-3
• Mol File: 57981-99-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 320.9°Cat760mmHg
• Flash Point: 135.5°C
• Appearance: /
• Density: 1.294g/cm³
• Vapor Pressure: 0.000308mmHg at 25°C
• Refractive Index: 1.521
• CAS DataBase Reference: 2-chloro-1,4-phenylene diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-1,4-phenylene diacetate(57981-99-4)
• EPA Substance Registry System: 2-chloro-1,4-phenylene diacetate(57981-99-4)

Safety Data

• Hazardous Substances Data: 57981-99-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H9ClO4/c1-6(12)14-8-3-4-10(9(11)5-8)15-7(2)13/h3-5H,1-2H3

Upstream product

• 695-99-8 2-Chloro-1,4-benzoquinone 
• 108-24-7 acetic anhydride 
• 615-67-8 chloro-p-hydroquinone 
• 106-51-4 p-benzoquinone 
• 75-36-5 acetyl chloride 
• 60-29-7 diethyl ether 
• 123-91-1 1,4-dioxane 

Downstream Products

• 90110-31-9 1-(4-chloro-2,5-dihydroxy-phenyl)-ethanone 
• 62489-80-9 4-acetoxy-2-chlorophenol 

Relevant articles and documents

Properties of chlorinated dihydroxybenzenes - components of pulp bleaching effluents

Gas chromatography and mass spectrometry data are given for the chlorodihydroxybenzenes which are components of wood pulp bleaching effluents and biologically-treated effluents, and are proposed intermediates in the chlorination of humic acids. The chlorohydroxybenzenes include the nine chlorocatechols, the six chlorohydroquinones and the seven known chlororesorcinols. The 22 chlorinated compounds were generally well separated on a phenyl methyl silicone column with the exception of three dichloro compounds. The chloro compounds with the same level of chlorine substitution were not able to be distinguished on the basis of their electron impact mass spectra.