17419-96-4

Upstream product

• 134-20-3 2-carbomethoxyaniline 

Downstream Products

• 39269-90-4 2-((E)-(7R,11R)-3,7,11,15-Tetramethyl-hexadec-2-enylamino)-benzoic acid methyl ester 
• 39270-24-1 2-[2,3-Dimethoxy-5-methyl-4-oxo-cyclohexa-2,5-dien-(E)-ylideneamino]-benzoic acid methyl ester 
• 39269-91-5 2-(4-Hydroxy-2,3-dimethoxy-5-methyl-phenylamino)-benzoic acid methyl ester 
• 1338332-43-6 C₁₈H₁₉NO₂ 
• 61144-90-9 C₁₅H₁₂N₂O₄ 

Relevant academic research and scientific papers

Substituted N-aryl alk-1-enesulfinamides: Preparation, properties and conversion into the corresponding indole compounds [1]

Reaction of vinylic organometallic derivatives with N-sulfinyl arenamines 2 affords the title sulfinamides 3. On heating their solutions in selected solvents to 80-124 °C, these sulfinamides are converted into the corresponding indoles 6, probably via a [3.3]-sigmatropic rearrangement to intermediates VIII which undergo an intramolecular carbophilic reaction of the nitrogen atom with the neighboring sulfine group, followed by elimination of HSOH. The triethyloxonium tetrafluoroborate- or boron trifluoride etherate catalyzed conversion 3 → 6 can be carried out at a much lower temperature. Elsevier,.

Oral hypoglycemic agents: 1(2 carboxyphenyl)pyrroles

A series of 1 (2 carboxyphenyl) pyrroles and their cyclized derivatives, pyrrolo [1,2 a]indoles, was synthesized and screened for hypoglycemic activity in rats. 1 (2 Carboxy 3 chlorophenyl) pyrrole was the most active, but had side effects.