144242-09-1

Basic information

• Product Name: 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester
• Synonyms: 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester;1-Cycloheptene-1-carboxylic acid, 2-[[(trifluoroMethyl)sulfonyl]oxy]-, ethyl ester;Ethyl 2-(((trifluoroMethyl)sulfonyl)oxy)cyclohept-1-enecarboxylate
• CAS NO: 144242-09-1
• Molecular Formula: C₁₁H₁₅F₃O₅S
• Molecular Weight: 316.29
• Mol File: 144242-09-1.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• Density: 1.37
• CAS DataBase Reference: 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester(144242-09-1)
• EPA Substance Registry System: 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester(144242-09-1)

Safety Data

• Hazardous Substances Data: 144242-09-1(Hazardous Substances Data)

Usage

General Description

The chemical "2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid ethyl ester" is an organic compound with the molecular formula C12H15F3O4S. It is an ethyl ester derivative of 2-[[(Trifluoromethyl)sulfonyl]oxy]-1-cycloheptene-1-carboxylic acid, which is a carboxylic acid containing a cycloheptene ring. The compound contains a trifluoromethylsulfonyl group, which is a functional group often used in organic synthesis. It is likely to have applications in the field of organic chemistry, potentially as a reagent or intermediate in the synthesis of other compounds. The specific properties and uses of this compound would depend on further testing and research.

Upstream product

• 774-05-0 ethyl cycloheptanone-2-carboxylate 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 
• 52784-32-4 2-(methoxycarbonyl)cycloheptanone 

Downstream Products

• 189271-65-6 ethyl 2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]cyclohept-1-enecarboxylate 
• 181303-15-1 2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]-cyclohept-1-enecarbaldehyde 
• 189271-95-2 2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]cyclohept-1-enemethanol 
• 189272-30-8 methyl (E,E)-3-methyl-5-[2-[(E)-2-(2,6,6-trimethylcyclohex-1-enyl)ethenyl]cyclohept-1-enyl]penta-2,4-dienoate 

Relevant articles and documents

Preparation method of sulfydryl alkenyl ester compound

The invention relates to a preparation method of a sulfydryl alkenyl ester compound, belongs to the field of organic chemical synthesis, and aims to solve the problems of high risk of large-scale production and the like, and the synthesis route provided b

CYLCOALKENYL DERIVATIVES USEFUL AS AGONISTS OF THE GPR120 AND /OR GPR40 RECEPTORS

The present invention is directed to cycloalkenyl derivatives, pharmaceutical compositions containing them and their use in the treatment of disorders and conditions modulated by the GPR120 and / or GPR40 receptors. 5 More particularly, the compounds of the present invention are agonists of GPR120 and / or GPR40, useful in the treatment of, for example, obesity, Type II Diabetes Mellitus, dyslipidemia, etc.

Catalytic enantioselective nazarov cyclization: Construction of vicinal all-carbon-atom quaternary stereocenters

The diastereoselective asymmetric synthesis of vicinal all-carbon-atom quaternary stereocenters is a challenging problem in organic synthesis for which only few solutions have been described. A catalytic asymmetric Nazarov cyclization of fully substituted dienones that provides cyclopentenone derivatives with vicinal quaternary stereocenters in high optical purity and as single diastereoisomers is now reported.