13169-71-6

Basic information

• Product Name: (4-chlorophenyl)(1H-pyrrol-2-yl)methanone
• Synonyms: (4-chlorophenyl)(1H-pyrrol-2-yl)methanone;2-(4-CHLOROBENZOYL)PYRROLE;4-CHLOROPHENYL 2-PYRROLYL KETONE;2-(p-Chlorobenzoyl)pyrrole;Pyrrol-2-yl 4-chlorophenyl ketone
• CAS NO: 13169-71-6
• Molecular Formula: C₁₁H₈ClNO
• Molecular Weight: 205.65
• EINECS: 604-604-1
• Mol File: 13169-71-6.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (4-chlorophenyl)(1H-pyrrol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chlorophenyl)(1H-pyrrol-2-yl)methanone(13169-71-6)
• EPA Substance Registry System: (4-chlorophenyl)(1H-pyrrol-2-yl)methanone(13169-71-6)

Safety Data

• Hazardous Substances Data: 13169-71-6(Hazardous Substances Data)

Usage

General Description

(4-chlorophenyl)(1H-pyrrol-2-yl)methanone is a chemical compound that consists of a 4-chlorophenyl group and a 1H-pyrrol-2-yl group linked to a methanone group. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This chemical may have various properties, including being a solid at room temperature with a specific melting point and boiling point. Additionally, it may exhibit certain chemical reactivity and potential health hazards, so proper handling and storage are important. Overall, (4-chlorophenyl)(1H-pyrrol-2-yl)methanone has a variety of potential uses in the field of organic chemistry and drug synthesis.

Upstream product

• 74-11-3 para-chlorobenzoic acid 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 20671-52-7 lithium pyrrolide 
• 104-88-1 4-chlorobenzaldehyde 
• 38480-28-3 2-bromo-1H-pyrrole 
• 873-76-7 para-Chlorobenzyl alcohol 
• 109-97-7 pyrrole 
• 58948-38-2 2-(4-Chlorophenyl)-1,3-benzoxathiolium tetrafluoroborate 
• 122-01-0 4-chloro-benzoyl chloride 
• 112816-54-3 2-[2-(4-Chloro-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 
• 132371-47-2 2-[2-(4-Chloro-phenyl)-benzo[1,3]dithiol-2-yl]-1H-pyrrole 
• 62128-38-5 (4-chlorophenyl)-(1H-pyrrol-3-yl)methanone 
• 19202-04-1 N-(4-chlorobenzoyl)morpholine 
• 14989-30-1 hypochloric acid 

Downstream Products

• 129055-90-9 [1-(2-Chloromethyl-benzyl)-1H-pyrrol-2-yl]-(4-chloro-phenyl)-methanone 
• 129055-80-7 (1-{2-[2-(4-Chloro-benzoyl)-pyrrol-1-ylmethyl]-benzyl}-1H-pyrrol-2-yl)-(4-chloro-phenyl)-methanone 
• 147088-92-4 [4-(4-Chloro-benzoyl)-1H-pyrrol-2-yl]-(4-chloro-phenyl)-methanone 
• 154047-00-4 (1-Allyl-1H-pyrrol-2-yl)-(4-chloro-phenyl)-methanone 
• 62128-38-5 (4-chlorophenyl)-(1H-pyrrol-3-yl)methanone 
• 86770-47-0 2-(p-chlorobenzyl)pyrrole 
• 154047-16-2 (4-Chloro-phenyl)-(1H-pyrrol-2-yl)-methanol 
• 157847-12-6 2-chloro-1-[5-(4-chlorobenzoyl)-1H-pyrrol-3-yl]ethanone 
• 154047-19-5 (1-Allyl-1H-pyrrol-2-yl)-(4-chloro-phenyl)-methanol 
• 22112-77-2 5,10,15,20-tetra-(4-chlorophenyl)porphyrin 
• 129055-85-2 11-(4-Chloro-phenyl)-5H-benzo[e]pyrrolo[1,2-a]azepine 
• 1528751-57-6 ethyl {2-[(4-chlorophenyl)carbonyl]-1H-pyrrol-1-yl}acetate 

Relevant articles and documents

Synthesis method of 2-aromatic acyl pyrrole compounds

The invention relates to the field of organic synthesis, and discloses a synthesis method of 2-aromatic acyl pyrrole compounds, wherein the synthesis method comprises the steps: taking an N-aromatic acyl pyrrole compound as a raw material, and carrying ou

Method for synthesizing drug intermediate pyrrolidone compound

The invention relates to a method for synthesizing a pyrrolidone compound which can be used as a drug intermediate as shown in a formula (III). The method comprises the following steps: reacting a compound as shown in a formula (I) with a compound as shown in a formula (II) in the presence of a catalyst, an organic ligand, an oxidant, an adjuvant and alkali in an organic solvent under a nitrogen atmosphere, and performing post-treatment after the reaction is completed to obtain the compound as shown in the formula (III), wherein R is H, C1-C6 alkyl, C1-C6 alkoxy, halogen or nitro. According to the method, a comprehensive reaction system of catalyst, ligand, oxidant, alkali and solvent is adopted, so that a target product is obtained with high yield. The pyrrolidone compound has an excellent application prospect and industrial production potential in the technical field of organic synthesis, especially drug intermediate synthesis.

Synthesis of a new compound family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5] triazepin-4(5H)-ones

Representatives of a new family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5]triazepin- 4(5H)-ones have been synthesized at our laboratory as bioisosters of biologically active 1-aryl-2,3-benzodiazepine-4-ones. The efficient synthetic route described applies the synth