33369-47-0

Basic information

• Product Name: ethyl 1,4-dimethyl-1H-pyrrole-2-acetate
• Synonyms: ethyl 1,4-dimethyl-1H-pyrrole-2-acetate;1,4-Dimethyl-1H-pyrrole-2-acetic acid ethyl ester;1H-Pyrrole-2-acetic acid, 1,4-diMethyl-, ethyl ester;ethyl 2-(1,4-dimethyl-1H-pyrrol-2-yl)acetate
• CAS NO: 33369-47-0
• Molecular Formula: C₁₀H₁₅NO₂
• Molecular Weight: 181.2316
• EINECS: 251-478-4
• Mol File: 33369-47-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 261.4°C at 760 mmHg
• Flash Point: 111.9°C
• Appearance: /
• Density: 1.02g/cm³
• Vapor Pressure: 0.0116mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: ethyl 1,4-dimethyl-1H-pyrrole-2-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1,4-dimethyl-1H-pyrrole-2-acetate(33369-47-0)
• EPA Substance Registry System: ethyl 1,4-dimethyl-1H-pyrrole-2-acetate(33369-47-0)

Safety Data

• Hazardous Substances Data: 33369-47-0(Hazardous Substances Data)

Usage

General Description

Ethyl 1,4-dimethyl-1H-pyrrole-2-acetate is a chemical compound with the molecular formula C10H15NO2. It is a pyrrole derivative, which is a type of organic compound containing a five-membered ring with one nitrogen atom. This chemical is an acetate ester, meaning that it contains an acetyl group attached to an ethyl group, and it also has two methyl groups attached to the pyrrole ring. Ethyl 1,4-dimethyl-1H-pyrrole-2-acetate is used in the synthesis of various pharmaceuticals and fine chemicals, and it may also have potential applications in the field of organic electronics. It is important to handle this chemical with care and follow proper safety precautions when working with it.

InChI:InChI=1/C10H15NO2/c1-4-13-10(12)6-9-5-8(2)7-11(9)3/h5,7H,4,6H2,1-3H3

Upstream product

• 82875-55-6 3-(Ethoxycarbonyl)-1,4-dimethyl-1H-pyrrole-2-acetic Acid 
• 33369-45-8 3-carboxy-1,4-dimethyl-1H-pyrrole-2-acetic acid 
• 33369-46-9 Ethyl 3-Carboxy-1,4-dimethyl-1H-pyrrole-2-acetate 
• 33369-26-5 1,4-dimethyl-3-carbethoxy-pyrrole-2-acetic acid ethyl ester 
• 140-88-5 ethyl acrylate 

Downstream Products

• 108832-28-6 [5-(1-Benzyl-1H-pyrrole-2-carbonyl)-1,4-dimethyl-1H-pyrrol-2-yl]-acetic acid 
• 33369-50-5 ethyl 5-benzoyl-1,4-dimethylpyrrole-2-acetate 
• 200496-31-7 N-{3-fluoro-4-[5-benzoyl-1-methyl-1H-pyrrol-2-ylmethyl]-phenyl}-2-(acetoxy)ethanesulfonamide 
• 33369-30-1 ethyl 5-(4-chlorobenzoyl)-1,4-dimethylpyrrole-2-acetate 
• 99231-49-9 Ethyl 5-[(4-chlorophenyl)(methylimino)methyl]-1,4-dimethyl-1H-pyrrole-2-acetate Perchlorate 
• 64541-13-5 ethyl 1,4-dimethyl-5-(p-nitrobenzoyl)pyrrole-2-acetate 
• 157847-02-4 5-(2,4-dichlorobenzoyl)-1,4-dimethyl-1H-pyrrole-2-acetic acid 
• 157847-03-5 (2,4-dichlorophenyl)(1,3,5-trimethyl-1H-pyrrol-2-yl)-methanone 
• 157847-04-6 2-chloro-1-[5-(2,4-dichlorobenzoyl)-1,2,4-trimethyl-1H-pyrrol-3-yl]-ethanone 

Relevant articles and documents

Synthesis of Pyrroles through Rhodium(III)-Catalyzed Reactions of Allylamines and Alkenes

Pyrrole derivatives are generated in reactions of allylamines with alkenes that are promoted by a Rh(III) catalyst in the presence of AgOAc. This process, which involves chelation assisted C-H bond activation and N-annulation, is applied to a three step synthesis of Zomepirac.

Selective Decarbethoxylation of Ethyl 1,4-Dimethyl-3-(ethoxycarbonyl)-1H-pyrrole-2-acetate in 85percent Phosphoric Acid

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Selective Hydrolysis-Decarboxylation of Ethyl 1,4-Dimethyl-3-(ethoxycarbonyl)-1H-pyrrole-2-acetate

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