59897-92-6

Basic information

• Product Name: ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate
• Synonyms: ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate;ethyl 4，6，6-trichloro-3，3-dimethyl hexeno-5-ate;4,6,6-Trichloro-3,3-dimethyl-5-hexenoic acid ethyl ester
• CAS NO: 59897-92-6
• Molecular Formula: C₁₀H₁₅Cl₃O₂
• Molecular Weight: 273.60
• Mol File: 59897-92-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 383.71°C (rough estimate)
• Flash Point: 112.2°C
• Appearance: /
• Density: 1.3075 (rough estimate)
• Vapor Pressure: 0.000755mmHg at 25°C
• Refractive Index: 1.4521 (estimate)
• CAS DataBase Reference: ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate(59897-92-6)
• EPA Substance Registry System: ethyl 4,6,6-trichloro-3,3-dimethyl-hex-5-enoate(59897-92-6)

Safety Data

• Hazardous Substances Data: 59897-92-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H15Cl3O2/c1-4-15-9(14)6-10(2,3)7(11)5-8(12)13/h5,7H,4,6H2,1-3H3

Downstream Products

• 55701-05-8 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid 
• 59609-49-3 ethyl 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate 
• 63142-57-4 ethyl (+/-)-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate 
• 63142-56-3 ethyl (+/-)-cis-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate 

Relevant articles and documents

Method of producing cyclopropanecarboxylic acids and esters

Novel γ-lactone derivatives are provided. These lactone derivatives, when reacted with hydrogen halide in alcohol, yield γ-halogeno-δ-unsaturated carboxylic acid esters. This ring-opening process is useful for the purpose of increasing the yield of pyrethrin analogs which are of value as insecticides and agricultural chemicals. Thus, the γ-lactone derivatives by-produced in the production process for dihalogenovinyl chrysanthemumates are caused to undergo ring-opening reaction to yield the corresponding γ-halogeno-δ-unsaturated carboxylic acid esters which are important intermediates for said pyrethrin analogs.