69563-07-1

Basic information

• Product Name: 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetimidoyl chloride
• Synonyms: 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetimidoyl chloride
• CAS NO: 69563-07-1
• Molecular Weight: 275.581
• Mol File: 69563-07-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetimidoyl chloride(69563-07-1)
• EPA Substance Registry System: 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetimidoyl chloride(69563-07-1)

Safety Data

• Hazardous Substances Data: 69563-07-1(Hazardous Substances Data)

Upstream product

• 2946-73-8 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetamide 
• 98-16-8 3-trifluoromethylaniline 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 1448786-48-8 C₁₈H₁₀F₆N₂O 
• 392-36-9 C₉H₄F₆N₂ 
• 392-36-9 2,4-bis(trifluoromethyl)-1H-benzo[d]imidazole 
• 399-69-9 2,5-bis(trifluoromethyl)-1H-benzo[d]imidazole 
• 1353778-33-2 2,2,2-trifluoro-N'-(3-(trifluoromethyl)phenyl)acetamidine 
• 1236874-56-8 C₉H₅F₆NS 
• 2946-73-8 2,2,2-trifluoro-N-(3-(trifluoromethyl)phenyl)acetamide 
• 1357114-27-2 5-methyl-2-(trifluoromethyl)-1-(3-(trifluoromethyl)phenyl)-1H-imidazole 

Relevant articles and documents

Annulation of CF3-Imidoyl Sulfoxonium Ylides with 1,3-Dicarbonyl Compounds: Access to 1,2,3-Trisubstituted 5-Trifluoromethylpyrroles

A lithium-bromide-promoted nucleophilic substitution/annulation cascade reaction between CF3-imidoyl sulfoxonium ylides and 1,3-dicarbonyl compounds has been established, and the corresponding 1,2,3-trisubstituted 5-trifluoromethylpyrroles have been obtai

Synthesis of new (trifluoromethyl)-1H-benzo[e][1,2,4]triazolo[1,2-a][1,2,4]triazine-1,3(2H)-diones and (trifluoromethyl)benzo[5,6][1,2,4]triazino [1,2-b]phthalazine-8,13-diones

In this paper we investigated reactions of urazole and phthalazine with N-(aryl)-2,2,2-trifluoroacetimidoyl chloride derivatives. Results showed that when imidoyl chloride derivative has a fluorine atom at ortho position (3a–c), in two steps under a Ssub

One-pot synthesis of novel (2R,4S)-N-aryl-4-hydroxy-1-(2,2,2-trifluoroacetyl) pyrrolidine-2-carboxamides via TiO 2 -NPs and Pd(PPh3)2Cl2 catalysts and investigation of their biological activities

Abstract: A new class of (2R,4S)-N-aryl-4-hydroxy-1-(2,2,2-trifluoroacetyl)pyrrolidine-2-carboxamide compounds was synthesized by a facile one-pot reaction of trans-4-hydroxy proline and trifluoroacetimidoyl chlorides in the presence of TiO 2-n