26173-92-2

Basic information

• Product Name: 5-methyl-1H-pyrrole-2-carbonitrile(SALTDATA: FREE)
• Synonyms: 5-methyl-1H-pyrrole-2-carbonitrile(SALTDATA: FREE);5-Methyl-1H-pyrrole-2-carbonitrile
• CAS NO: 26173-92-2
• Molecular Formula: C6H6N2
• Molecular Weight: 106.12524
• Mol File: 26173-92-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 266.8±20.0 °C(Predicted)
• Appearance: /
• Density: 1.11±0.1 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.90±0.50(Predicted)
• CAS DataBase Reference: 5-methyl-1H-pyrrole-2-carbonitrile(SALTDATA: FREE)(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methyl-1H-pyrrole-2-carbonitrile(SALTDATA: FREE)(26173-92-2)
• EPA Substance Registry System: 5-methyl-1H-pyrrole-2-carbonitrile(SALTDATA: FREE)(26173-92-2)

Safety Data

• Hazardous Substances Data: 26173-92-2(Hazardous Substances Data)

Usage

General Description

5-methyl-1H-pyrrole-2-carbonitrile is a chemical compound with the molecular formula C6H6N2. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. The compound is a pyrrole derivative, which is a heterocyclic aromatic organic compound. It has applications in the pharmaceutical industry as a building block for the synthesis of drugs. The chemical is also used as a starting material in the production of agrochemicals and dyes. It is important to handle this compound with care, as it can be potentially hazardous if not handled properly.

Upstream product

• 6624-45-9 5-methyltetrazolo[1,5-a]pyridine 
• 1192-79-6 formyl-2 methyl-5 pyrrole 
• 858448-70-1 C₆H₈N₂O 
• 821-10-3 1,4-Dichloro-2-butyne 
• 90877-70-6 ethyl 2-acetamido-2-cyanoacetate 

Relevant articles and documents

Facile synthesis of pyrazoles and pyrroles via thermolysis of tetrazolo[1,5-b]pyridazines, tetrazolo[1,5-a]pyrimidines and tetrazolo [1,5- a]pyridines

A simple and high yielding preparation of pyrazoles and pyrroles is described. Thermolysis of tetrazolo[1,5b]pyridazines, tetrazolo[1,5- a]pyrimidines and tetrazolo[1,5-a]pyridines allowed easy ring contraction thus providing a facile preparation of cyano

Unusual oxidation in the course of synthesis of V-confused nickel tetrahydrobilins

TV-confused Tetrahydrobilins rac-16 and rac-17 were prepared to investigate their cyclization directed to the formation of N-confused chlorins. For achieving the desired cyclization the 5'-position of rac-16 respectively rac-17 was activated by an electron withdrawing cyano function and their 2'-positions were blocked by a methyl group. In addition, the insertion of Ni(II) was accomplished for exercising a template effect during the cyclization process, but the formed nickel complexes rac-18 and rac-19 underwent oxidation to yield oxo-tetrahydrobilins rac-20 and rac-21. The Japan Institute of Heterocyclic Chemistry.