170366-90-2

Basic information

• Product Name: Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI)
• Synonyms: Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI);2,2,2-trifluoro-1-(1H-indol-5-yl)-ethanone;2,2,2-trifluro-1-(1H-indol-5-yl)-ethanone;Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)-
• CAS NO: 170366-90-2
• Molecular Formula: C₁₀H₆F₃NO
• Molecular Weight: 213.1559496
• Product Categories: ACETYLHALIDE
• Mol File: 170366-90-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 308.6±37.0 °C(Predicted)
• Appearance: /
• Density: 1.423±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 15.45±0.30(Predicted)
• CAS DataBase Reference: Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI)(170366-90-2)
• EPA Substance Registry System: Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI)(170366-90-2)

Safety Data

• Hazardous Substances Data: 170366-90-2(Hazardous Substances Data)

Usage

General Description

Ethanone, 2,2,2-trifluoro-1-(1H-indol-5-yl)- (9CI) is a chemical compound with the molecular formula C10H7F3NO. It is also known as 2,2,2-trifluoro-1-(1H-indol-5-yl)ethan-1-one and is classified as a ketone derivative. This chemical is characterized by the presence of a trifluoromethyl group and an indol-5-yl substituent. It is often used in organic synthesis and pharmaceutical research due to its unique structure and potential pharmacological properties. Additionally, it is considered a valuable building block in the development of new compounds for various applications in the fields of medicine and drug discovery.

Upstream product

• 10075-50-0 5-bromo-1H-indole 
• 340-07-8 N-(trifluoroacetyl)piperidine 
• 181820-18-8 S-(tert-butyl)trifluorothioacetate 
• 144104-59-6 1H-indole-5-boronic acid 
• 407-25-0 trifluoroacetic anhydride 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 170366-91-3 2,2,2-trifluoro-1-[1-di(4-fluorophenyl)methylindol-5-yl]-1-ethanone 

Relevant articles and documents

Comprehensive synthesis of photoreactive (3-trifluoromethyl)diazirinyl indole derivatives from 5- and 6-trifluoroacetylindoles for photoaffinity labeling

5- and 6-trifluoromethyldiazirinyl indoles were synthesized from corresponding bromoindole derivatives for the first time. They acted as mother skeletons for the comprehensive synthesis of various bioactive indole metabolites. These can be used in biologi

Indol-containing beta-agonists, methods for the preparation thereof and their use as pharmaceutical compositions

The present invention relates to new beta-agonists of general formula (I) wherein the groups R1 and R2 have the meanings given in the claims and specification, the tautomers, racemates, enantiomers, diastereomers, solvates, hydrates,