10333-68-3

Usage

Uses

Due to the limited information available on the specific applications of 1-(2-Carboxyphenyl)pyrrole, the following uses are inferred based on its chemical properties and potential:
Used in Research and Development:
1-(2-Carboxyphenyl)pyrrole is used as a research compound for studying its chemical properties, reactivity, and potential applications in various fields. Its aromatic and acidic nature makes it a candidate for further investigation in chemical synthesis and material science.
Used in Chemical Synthesis:
1-(2-Carboxyphenyl)pyrrole can be used as a building block or intermediate in the synthesis of more complex organic compounds, such as pharmaceuticals, agrochemicals, or specialty chemicals. Its carboxylic acid group allows for various chemical reactions, including esterification, amidation, and condensation, which can be exploited in the development of new molecules with desired properties.
Used in Material Science:
The aromatic nature of 1-(2-Carboxyphenyl)pyrrole suggests potential applications in the development of new materials with specific properties, such as conductivity, stability, or selectivity. Its incorporation into polymers, coatings, or other materials could lead to innovative products with improved performance.

InChI:InChI=1/C11H9NO2/c13-11(14)9-5-1-2-6-10(9)12-7-3-4-8-12/h1-8H,(H,13,14)

Upstream product

• 635-90-5 1-phenylpyrrole 
• 124-38-9 carbon dioxide 
• 10333-67-2 methyl 2-(1H-pyrrol-1-yl)benzoate 
• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 118-92-3 anthranilic acid 
• 134-20-3 2-carbomethoxyaniline 

Downstream Products

• 133662-28-9 chlorure de 2-(1-pyrrolyl)benzoyle 
• 1400797-60-5 C₁₈H₁₆N₂O 
• 6025-68-9 pyrrolo<1,2-a>quinoxalin-4(5H)-one 
• 1078711-94-0 N-{(3-exo)-8-[(6-fluoro-2-naphthyl)methyl]-8-azabicyclo[3.2.1]oct-3-yl}-2-(1H-pyrrol-1-yl)benzamide 
• 610794-06-4 N-indan-2-yl-N-(3-methyl-benzyl)-2-pyrrol-1-yl-benzamide 
• 279256-35-8 tert-butyl-2(R)-[(3,4-methylendioxybenzyl)-(2,6-dimethyl-4-methoxybenzenesulfonyl)amino]-3-[(2-pyrrol-1-yl)phenylcarbonylamino]-propionate 
• 133662-32-5 2-(1-pyrrolyl)diazoacetophenone 
• 55540-39-1 acide 2-(1-pyrrolyl)phenyl acetique 
• 140119-63-7 9-(4-methylcyclohexylamino)-9H-pyrrolo<1,2-a>indole 
• 140119-48-8 N-(α-methylbenzyl)-9H-pyrrolo<1,2-a>indol-9-imine 
• 140119-49-9 N-(4-methylcyclohexyl)-9H-pyrrolo<1,2-a>indol-9-imine 
• 140119-41-1 N-(2-(1-pyrrolyl)benzoyl)morpholine 
• 101125-93-3 2-(9H-Pyrrolo[1,2-a]indol-9-ylamino)-ethanol 
• 101125-88-6 2-[Pyrrolo[1,2-a]indol-(9Z)-ylideneamino]-ethanol 

Relevant academic research and scientific papers

Copper(II)-mediated regioselective N-arylation of pyrroles, indoles, pyrazoles and carbazole via dehydrogenative coupling

A copper(ii)-mediated regioselective N-arylation of azoles has been developed using 8-aminoquinoline amide as a directing group. This reaction shows a broad substrate scope with different azoles such as pyrroles, indoles, pyrazoles and carbazole with good

Br?nsted Acid-Catalyzed Asymmetric Ring-Closing Alkylation of Inert N-substituted Pyrroles with α, β-Unsaturated Ketones

A Chiral Br?nsted acid catalyzed asymmetric intramolecular ring-closing alkylation of inert pyrroles with α, β-unsaturated ketones has been developed. This approach gave a wide range of 4-phenyl-4,5-dihydro-6H-benzo[f]pyrrolo[1,2-a]azepin-6-ones in high yields with good enantioselectivities under mild reaction conditions. (Figure presented.).

Active manganese dioxide promoted cyclization of ortho-(1H-pyrrol-1-yl)aryl and heteroaryl carboxylic acids to 5H-pyrrolo[1,2-a][3,1]benzoxazin-5-one derivatives

The hitherto unknown lactone 5H-pyrrolo[1,2-a][3,1]benzoxazin-5-one and six of its substituted derivatives have been prepared by active manganese dioxide promoted oxidative cyclization of the corresponding 2-(1H-pyrrol-1-yl)benzoic acids, under mild conditions, in moderate yields. The method was successfully extended to the cyclization of some ortho-(1H-pyrrol-1-yl)heteroaryl carboxylic acids and 2-(1H-indol-1-yl)benzoic acids.

Tricyclic oxime ethers

The present invention relates to compounds of formula (I): STR1 wherein A, x, y, R1, R2 and R3 are as defined in the description. The compounds are useful for treating diseases requiring a selective serotonin reuptake site

N-phenylpyrrole: A kinetic, though not thermodynamic preference for dilithiation

Under appropriate conditions the clean preparation of either the α-monolithiated or the o,α-dilithiated derivative of N-phenylpyrrole is possible. In the latter case, the first deprotonation occurs at the α-position. Dimetalation is kinetically but not thermodynamically favored.

The Preparation of 2,3-Dihydro-1H-pyrroloindole, 2,3-Dihydro-9-methyl-1H-pyrroloindole, 1,2,2a,3,4,5-hexahydropyrrolocarbazole, and 2,3,3a,4,5,6-hexahydro-1H-pyridocarbazole

Several routes for the preparation of the four compounds listed in the title have been investigated to decide on methods suitable for obtaining the materials in quantity.

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.