634172-95-5

Usage

Molecular structure

The compound has a pyrrole backbone with a methyl ester group, a bromophenylmethylene group, and a methylamino functional group.

Molecular geometry

The (5Z)notation indicates that the molecule has a specific geometry, with the double bond located between the carbon atoms of the pyrrole ring.

Potential applications

The compound may have potential uses in pharmaceuticals, agrochemicals, and materials science.

Further investigation

The precise structure and properties of the compound would require further investigation to fully understand its potential uses and effects.

Upstream product

• 97066-53-0 methyl 5-[bromo(phenyl)methylidene]-2,5-dihydro-4-methoxy-2-oxo-1H-1H-pyrrole-3-carboxylate 
• 74-89-5 methylamine 

Downstream Products

• 634173-04-9 methyl 4,5-dihydro-1,4-dimethyl-2,2,5-trioxo-3-phenyl-1H-2λ⁶-pyrrolo[3,2-c]isothiazole-6-carboxylate 
• 634173-01-6 methyl 4,5-dihydro-1-methyl-2,2,5-trioxo-3-phenyl-1H-2λ⁶-pyrrolo[3,2-c]isothiazole-6-carboxylate 
• 634173-24-3 4,5-dihydro-1,4-dimethyl-5-oxo-3-phenyl-1H-pyrrolo[3,2-c]isothiazole-6-carboxylic acid 
• 634173-13-0 methyl 4,5-dihydro-1,4-dimethyl-5-oxo-3-phenyl-1H-pyrrolo[3,2-c]isothiazole-6-carboxylate 
• 634173-10-7 methyl 4,5-dihydro-1-methyl-5-oxo-3-phenyl-1H-pyrrolo[3,2-c]isothiazole-6-carboxylate 
• 634173-28-7 1,4-dimethyl-3-phenyl-1H-pyrrolo[3,2-c]isothiazol-5(4H)-one 
• 528881-26-7 methyl 1,2,4,5-tetrahydro-1-methyl-2,5-dioxo-3-phenyl-2λ⁴-pyrrolo[3,2-c]isothiazole-6-carboxylate 

Relevant academic research and scientific papers

Metal complexes of functionalized sulfur-containing ligands: Part XIX. Synthesis and reactions of new pyrroloisothiazoles

The title compounds were prepared starting from the dihydropyrrolones 4-6. Nucleophilic displacement and ring closure yielded the 1H-pyrrolo[3,2-c]isothiazol-5(4H)-ones 8 and 10. The fused systems formed salts with strong acids and electrophiles (15, 16), as well as with bases. Oxidation led either to S(2)-oxides (18a, 20a) or to the corresponding bicyclic sultams (18b, 20b), depending on the reaction conditions. The sulfinamide 18a was also obtained from the known 1,2-dithiolopyrrolone S-oxide 21 by a ring-opening/ring-closure reaction sequence. O-Methylation of 8 furnished the 'azafulvene' 17. The oxidative addition of [Pt(η2-C 2H4)L2] (24a: L = Ph3P,24b: L = 1/2 dppf. 24c: L = 1/2 (R,R)-diop) to 18a and 20a led to the cis-amido-sulfenato Pt complexes 25 and 26a-c, respectively.