774-18-5

Usage

Uses

Due to the lack of specific information on the applications of o-(trifluoromethyl)phenethylamine, it is not possible to provide a detailed list of its uses. However, as a member of the trifluoromethylbenzenes and phenethylamines classes, it may potentially be used in various chemical synthesis processes or as an intermediate in the production of pharmaceuticals or other organic compounds. Further research and development would be required to explore its potential applications and establish its safety and efficacy in specific industries.

InChI:InChI=1/C9H10F3N/c10-9(11,12)8-4-2-1-3-7(8)5-6-13/h1-4H,5-6,13H2

Upstream product

• 3038-47-9 2-(trifluoromethyl)phenylacetonitrile 

Downstream Products

• 934525-75-4 C₁₉H₂₇F₃N₂O₃ 
• 1180007-74-2 C₁₀H₉F₆NO₂S 
• 1373618-93-9 C₁₅H₁₃F₃N₂O 
• 1373618-69-9 C₁₆H₁₅F₃N₂O₂ 
• 120-72-9 indole 
• 1381861-21-7 C₁₅H₁₁F₃N₂O 
• 1381861-22-8 C₁₇H₁₅F₃N₂O₃ 
• 1427329-47-2 2-phenyl-N-{2-[2-(trifluoromethyl)phenyl]ethyl}acetamide 
• 1427329-51-8 2-(4-chlorophenyl)-N-{2-[2-(trifluoromethyl)phenyl]ethyl}acetamide 
• 1427329-52-9 2-(4-fluorophenyl)-N-{2-[2-(trifluoromethyl)phenyl]ethyl}acetamide 
• 1439537-71-9 2-(4-methoxyphenyl)-N-{2-[2-(trifluoromethyl)phenyl]ethyl}acetamide 
• 1439539-50-0 2-(3,4-dimethoxyphenyl)-N-{2-[2-(trifluoromethyl)phenyl]ethyl}acetamide 
• 1290619-73-6 N-{2-[2-(trifluoromethyl)phenyl]ethyl}-2-(3,4,5-trimethoxyphenyl)acetamide 
• 1440514-98-6 C₁₄H₁₃F₃N₂O₂S 

Relevant academic research and scientific papers

17a-HYDROXYLASE/C17,20-LYASE INHIBITORS

The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, A and n are as defined herein. A deuteriated derivative of the compound of Formula (I) is also provided.

17α-HYDROXYLASE/C17,20-LYASE INHIBITORS

The present invention provides compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, R6, A and n are as defined herein. A deuteriated derivative of the compound of Formula (I) is also provided.

Improved protocol for indoline synthesis via palladium-catalyzed intramolecular C(sp2)-H amination

An efficient method has been developed for the synthesis of indoline compounds from picolinamide (PA)-protected β-arylethylamine substrates via palladium-catalyzed intramolecular amination of ortho-C(sp2)-H bonds. These reactions feature high efficiency, low catalyst loadings, mild operating conditions, and the use of inexpensive reagents.

TETRAHYDROPYRANYL CYCLOPENTYL TETRAHYDROISOQUINOLINE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

The present invention is directed to compounds of the formula I: I(wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, X, n and the dashed line are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptor CCR-2.