17536-39-9

Basic information

• Product Name: ETHYL (5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE
• Synonyms: ETHYL (5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE;ETHYL 2-(5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE;Ethyl 5-Fluoro-2-methyl-3-indoleacetate
• CAS NO: 17536-39-9
• Molecular Formula: C₁₃H₁₄FNO₂
• Molecular Weight: 235.25
• Mol File: 17536-39-9.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: ETHYL (5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: ETHYL (5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE(17536-39-9)
• EPA Substance Registry System: ETHYL (5-FLUORO-2-METHYL-1H-INDOL-3-YL)ACETATE(17536-39-9)

Safety Data

• Hazardous Substances Data: 17536-39-9(Hazardous Substances Data)

Upstream product

• 823-85-8 4-fluorophenyhydrazine hydrochloride 
• 123-76-2 levulinic acid 
• 623-73-4 diazoacetic acid ethyl ester 
• 399-72-4 5-fluoro-2-methyl-1H-indole 
• 64-17-5 ethanol 
• 539-88-8 4-oxopentanoic acid ethyl ester 
• 371-14-2 4-fluorophenylhydrazine 

Downstream Products

• 851449-40-6 [5-fluoro-1-(4-fluorobenzenesulfonyl)-2-methyl-1H-indol-3-yl]acetic acid ethyl ester 
• 71987-67-2 2-(5-fluoro-2-methyl-1H-indol-3-yl)acetic acid 
• 1173195-01-1 {5-fluoro-1-[2-(4-fluorobenzenesulfonyl)benzyl]-2-methyl-1H-indolyl}acetic acid ethyl ester 
• 851449-46-2 [5-fluoro-2-methyl-1-(4-phenylsulfanyl-benzenesulfonyl)-1H-indol-3-yl]acetic acid ethyl ester 
• 881743-48-2 [5-fluoro-1-(4-fluorobenzyl)-2-methyl-1H-indol-3-yl]acetic acid 
• 881743-47-1 (1-benzyl-5-fluoro-2-methyl-1H-indol-3-yl)acetic acid 

Relevant articles and documents

Asymmetric Dearomatization of Indole Derivatives with N-Hydroxycarbamates Enabled by Photoredox Catalysis

Dearomatization of indoles provides efficient synthetic routes for substituted indolines. In most cases, indoles serve as nucleophiles. Reported here is an asymmetric dearomatization reaction of indole derivatives that function as electrophiles. The combination of a photocatalyst and chiral phosphoric acid open to air unlocks the umpolung reactivity of indoles, enabling their dearomatization with N-hydroxycarbamates as nucleophiles. A variety of fused indolines bearing intriguing oxy-amines were constructed in excellent yields with moderate to high enantioselectivities. Mechanistic studies show that the realization of two sequential single-electron transfer oxidations of the indole derivatives is key, generating the configurationally biased carbocation species while providing the source of stereochemical induction. These results not only provide an efficient synthesis of enantioenriched indoline derivatives, but also offer a novel strategy for further designing asymmetric dearomatization reactions.

ORGANIC COMPOUNDS

There are provided according to the invention compounds of formula (I) in free or salt form, wherein R1, R2, R4, R5, R6, D, X, W, m and n are as described in the specification, process for preparing t

4-AMINOMETHYL-1-ARYL-CYCLOHEXYLAMINE DERIVATIVES

The invention concerns 4-aminomethyl-1-aryl-cyclohexylamine derivatives, methods for producing same, medicines containing said compounds and the use of 4-aminomethyl-1-aryl-cyclohexylamine derivatives for producing medicines.