6203-15-2

Basic information

• Product Name: Acetamide, 2,2,2-trifluoro-N-(2-formylphenyl)-
• CAS NO: 6203-15-2
• Molecular Formula: C9H6F3NO2
• Molecular Weight: 217.147
• Mol File: 6203-15-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Acetamide, 2,2,2-trifluoro-N-(2-formylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, 2,2,2-trifluoro-N-(2-formylphenyl)-(6203-15-2)
• EPA Substance Registry System: Acetamide, 2,2,2-trifluoro-N-(2-formylphenyl)-(6203-15-2)

Safety Data

• Hazardous Substances Data: 6203-15-2(Hazardous Substances Data)

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 529-23-7 o-aminobenzaldehyde 
• 407-25-0 trifluoroacetic anhydride 
• 7772-99-8 stannous chloride 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 815632-53-2 4-{[2-(hydroxyiminomethyl)phenyl]-(2,2,2-trifluoroacetyl)amino}but-2(E)-enoic acid methyl ester 
• 452322-01-9 C₁₄H₁₂F₃NO₄ 
• 16498-68-3 1-(1-methyl-1H-indol-2-yl)ethanone 
• 1450994-91-8 ethyl (E)-4-[2,2,2-trifluoro-N-(2-formylphenyl)acetamido]but-2-enoate 
• 33054-18-1 ethyl 2-(quinolin-3-yl) acetate 
• 1450994-69-0 C₁₃H₁₅NO₃ 
• 104749-68-0 (1H-indol-2-yl)(4-methoxyphenyl)methanone 
• 1026-22-8 (4-chlorophenyl)(1H-indol-2-yl)methanone 
• 1026-21-7 (1H-indol-2-yl)(4-methyphenyl)methanone 
• 1022-86-2 2-benzoylindole 
• 370580-98-6 (1H-indol-2-yl)(3-methoxyphenyl)methanone 
• 912654-62-7 (2-bromophenyl)(1H-indol-2-yl)methanone 

Relevant articles and documents

A Au(i)-catalyzed hydrogen bond-directed tandem strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives

A gold-catalyzed hydrogen bond-directed tandem cyclization strategy to synthesize indeno-chromen-4-one and indeno-quinolin-4-one derivatives has been developed. The hydrogen bond existing between the hydroxyl group (or the amide group) and the carbonyl group played an essential role in controlling the selectivity, which was confirmed by both experimental and theoretical evidence.

A practical synthesis of 2-aroylindoles from N-(2-formylphenyl)trifluoro- acetamides in PEG-400

A one-pot and environmentally benign approach to the synthesis of highly functionalized 3-unsubstituted 2-aroylindoles is described. Moderate to good yields were obtained through the reaction of easily accessible N-(2-formylphenyl)trifluoroacetamides and

Cytotoxic compounds: derivatives of the pyrido [2,3,4-kl]acridine ring system

Compounds of formula (I), wherein X is selected from the group consisting of O, and NR3, where R3 represents a lower alkyl group; Y is selected from the group consisting of CH and N; R1 and R2 are independently