4310-42-3

Basic information

• Product Name: 1-(3-NITROPHENYL)-1H-PYRROLE
• Synonyms: 1-(3-NITROPHENYL)-1H-PYRROLE;BUTTPARK 96\50-06;3-Nitrophenyl-(1H)-pyrrole;1-(3-nitrophenyl)pyrrole
• CAS NO: 4310-42-3
• Molecular Formula: C₁₀H₈N₂O₂
• Molecular Weight: 188.18
• Mol File: 4310-42-3.mol
• Article Data: 19

Chemical Properties

• Melting Point: 72 °C
• Boiling Point: 319.8 °C at 760 mmHg
• Flash Point: 147.2 °C
• Appearance: /
• Density: 1.23 g/cm³
• Vapor Pressure: 0.000619mmHg at 25°C
• Refractive Index: 1.613
• PKA: -5.92±0.70(Predicted)
• CAS DataBase Reference: 1-(3-NITROPHENYL)-1H-PYRROLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-NITROPHENYL)-1H-PYRROLE(4310-42-3)
• EPA Substance Registry System: 1-(3-NITROPHENYL)-1H-PYRROLE(4310-42-3)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 4310-42-3(Hazardous Substances Data)

Usage

General Description

1-(3-NITROPHENYL)-1H-PYRROLE, also known as 3-Nitrophenyl-1H-pyrrole, is an organic compound with the formula C10H8N2O2. It is comprised of a pyrrole ring, a nitrogenous heterocyclic compound, attached to a nitrophenyl group. This chemical exhibits intense coloring and is often used in the synthesis of pharmaceuticals, dyes, and specialized materials due to its conductive and light absorbing properties. As with many nitrogenous organic compounds, careful handling is required due to potential explosiveness.

InChI:InChI=1/C10H8N2O2/c13-12(14)10-5-3-4-9(8-10)11-6-1-2-7-11/h1-8H

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Downstream Products

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Relevant articles and documents

Sulphonic acid functionalized porphyrin anchored with a: Meso -substituted triazolium ionic liquid moiety: A heterogeneous photo-catalyst for metal/base free C-C cross-coupling and C-N/C-H activation using aryl chloride under visible light irradiation

We report an easy process to synthesize sulphonic acid functionalized porphyrin, anchored with a meso-substituted triazolium ionic liquid moiety (SAFPTILM) for metal/base free C-C cross-coupling and C-N/C-H activation using aryl chloride under visible light irradiation. The acid strength has been measured based on the Hammett indicator. The SAFPTILM photocatalyst comprising 18 π-conjugated electronic systems with the chromophore substituents in the meso-position can provide rapid electronic conducting channels during photocatalysis under the irradiation of visible light. It was found that SAFPTILM is an efficient photocatalyst for the Heck, Sonogashira, Buchwald, Ullmann/Fittig coupling and C-H activation of phenols with different aryl chlorides in the absence of a base/noble metal, using 5 W LED (yellow) light under ambient conditions. The photocatalyst with low band gap (1.55 eV) comprising conjugation, favors coupling reaction of unactivated aryl chlorides, by easy excitation of electrons and transfer to the conjugated benzimidazolium based phenylenediamine support delaying the recombination of photoinduced electron-hole pairs.

Novel substituted benzoyl compound and its pharmaceutically acceptable salt and preparation method and application (by machine translation)

The invention relates to the general formula I shown novel substituted benzoyl compound and its pharmaceutically acceptable salt and preparation method and application. The invention also provides pharmaceutical compositions containing them, in vitro and in vivo anti-tumor effect results and acute toxicity study, the obtained anti-tumor drug model substituted benzoyl compound, has more excellent anti-tumor activity and safety, can be in the treatment of leukemia, lung cancer, colon cancer, ovarian cancer and renal carcinoma tumor in the application, so that the therapeutic window, so in the medical field as antitumor agents in the very application value. (by machine translation)

An efficient heterogeneous catalytic method for the N-arylation of pyrrole and other N-heterocycles

Abstract 4 ? molecular sieve modified with copper(0) or copper(II) is an efficient heterogeneous catalyst for the arylation of pyrrole and some other heterocycles with iodo- or bromoarenes, Cs2CO3 base and pyrrole (or DMF) solvent. The catalysts can be easily prepared and are reusable.