13712-55-5

Usage

Heterocyclic compound

A compound with a pyrrole ring structure 1H-Pyrrole, 2,5-dimethyl-1,3-diphenylis classified as a heterocyclic compound because it contains a ring structure with both carbon and nitrogen atoms.

Pyrrole ring structure

A five-membered ring with four carbon atoms and one nitrogen atom The core structure of 1H-Pyrrole, 2,5-dimethyl-1,3-diphenylconsists of a five-membered ring with four carbon atoms and one nitrogen atom, which is characteristic of pyrrole compounds.

Aromatic properties

Contributed by two methyl groups and three phenyl groups The presence of two methyl (CH3) and three phenyl (C6H5) groups attached to the pyrrole ring imparts aromatic properties to 1H-Pyrrole, 2,5-dimethyl-1,3-diphenyl-.

Building block in synthesis

Commonly used in the synthesis of various pharmaceuticals and organic compounds 1H-Pyrrole, 2,5-dimethyl-1,3-diphenylserves as an important building block or intermediate in the synthesis of a wide range of pharmaceuticals and organic compounds.

Potential applications

In the pharmaceutical and chemical industries Due to its diverse reactivity and structural features, 1H-Pyrrole, 2,5-dimethyl-1,3-diphenylhas potential applications in both the pharmaceutical and chemical industries for the development of new compounds and products.

Upstream product

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• 917-54-4 methyllithium 
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• 62-53-3 aniline 
• 67-64-1 acetone 
• 339987-27-8 4-phenyl-5-hexyn-2-one 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 866562-23-4 1-phenyl-3-(trimethylsilyl)prop-2-yn-1-yl acetate 
• 1833-53-0 2-(Trimethylsilyloxy)propene 
• 16169-88-3 1-phenylprop-2-ynyl acetate 
• 1134781-54-6 3-acetyl-4-phenyl-hexane-2,5-dione 
• 98-80-6 phenylboronic acid 
• 25234-74-6 3-phenylhexane-2,5-dione 

Relevant academic research and scientific papers

PYRROLE FORMATION FROM A (1-AZABUTADIENE)TRICARBONYLIRON(O) COMPLEX

The (1-azabutadiene)tricarbonyliron(O) complex 2 formed by selective complexation of the ECN isomer of the stereoisomeric mixture of 1-azabutadienes 1 reacts smoothly with methyl-lithium to give the 1,2,3,5-tetrasubstituted pyrrole 3.

Copper-Catalyzed Three-Component Reactions of α-Ketoaldehyde, 1,3-Dicarbonyl Compound, and Organic Boronic Acid in Water: A Route to 1,4-Diketones

A novel three-component reaction of α-ketoaldehydes, 1,3-dicarbonyl compounds, and organic boronic acids catalyzed by CuO in water has been developed to give a wide range of products containing 1,3/1,4-diketones. The method has some advantages such as the

One-pot highly efficient synthesis of substituted pyrroles and N-bridgehead pyrroles by zinc-catalyzed multicomponent reaction

A convenient zinc(ii) chloride-catalyzed regioselective propargylation/amination/cycloisomerization process has been developed for the synthesis of substituted pyrrole derivatives from propargylic acetates, enoxysilanes and primary amines. Various aromati

Novel ruthenium- and platinum-catalyzed sequential reactions: Synthesis of tri- and tetrasubstituted furans and pyrroles from propargylic alcohols and ketones

Two cats. in the same pot: The two catalysts [Cp*RuCl(μ2-SMe)2RuCp*Cl] (1) and PtCl2 (2) promote a sequence of catalytic cycles in the same medium. Trior tetrasubstituted furans or pyrroles are afforded in moderate to good yields with high regioselectivities from the catalyzed reactions of propargylic alcohols with ketones or with ketones and anilines, respectively (see scheme; cats.=catalysts).

Nucleophilic addition to tricarbonyliron(0) complexes of 1-aza-1,3-dienes and the production of pyrroles

The synthesis of a number of novel tricarbonyl(1-aza-1,3-diene)iron(0) complexes and their reactions with methyl-lithium are described. Addition proceeds under mild conditions and, in general, occurs at a metal carbonyl ligand; this leads via an unprecedented reaction to the production of several novel pyrroles.