6957-89-7

Basic information

• Product Name: ethyl dichloro(ethoxy)acetate
• Synonyms: Acetic acid, dichloroethoxy-, ethyl ester; Ethyl dichloro(ethoxy)acetate; Ethyl dichloroethoxyacetate
• CAS NO: 6957-89-7
• Molecular Formula: C₆H₁₀Cl₂O₃
• Molecular Weight: 201.0478
• Mol File: 6957-89-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 232.3°C at 760 mmHg
• Flash Point: 92.9°C
• Density: 1.254g/cm³
• Vapor Pressure: 0.0595mmHg at 25°C
• Refractive Index: 1.449
• CAS DataBase Reference: ethyl dichloro(ethoxy)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl dichloro(ethoxy)acetate(6957-89-7)
• EPA Substance Registry System: ethyl dichloro(ethoxy)acetate(6957-89-7)

Safety Data

• Hazardous Substances Data: 6957-89-7(Hazardous Substances Data)

Upstream product

• 95-92-1 oxalic acid diethyl ester 

Downstream Products

• 57267-03-5 1,1,1-triethoxyacetic acid ethyl ester 
• 74-87-3 methylene chloride 
• 66298-76-8 phosphonic dichloride 
• 75-00-3 chloroethane 
• 67538-59-4 ethyl phosphonofluoridate 
• 5524-56-1 ethyl 2-p-tolyl-2-oxoacetate 
• 66644-67-5 ethyl 2-methylbenzoylformate 
• 5524-57-2 ethyl 2-(2,4,6-trimethylphenyl)-2-oxoacetate 
• 74813-39-1 Chloro-(diphenoxy-phosphoryl)-ethoxy-acetic acid ethyl ester 
• 74813-40-4 P--N,N'-diphenylphosphonamidic diamide 
• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 62936-36-1 ethyl 2-(4-ethylphenyl)-2-oxoacetate 
• 80120-33-8 ethyl 2-(2,4-dimethylphenyl)-2-oxoacetate 
• 40140-16-7 ethyl (p-methoxyphenyl)oxoacetate 

Relevant articles and documents

Facile synthesis of 2,6-disubstituted benzobisthiazoles: Functional monomers for the design of organic semiconductors

(Chemical Equation Presented) The synthesis of several synthetically useful 2,6-disubstituted benzobisthiazoles is described. The method is based on the Lewis acid-catalyzed ring-closing reaction between substituted orthoesters and diamino benzene dithiol. The resulting benzobisthiazoles are obtained cleanly and in good yields. These materials are of interest for the development of new organic semiconductors.