I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
1-Methylpyrrole, can be used as organic synthetic materials, widely used in medicine. It is also used as a pharmaceutical intermediate.
TT Dang.; R Ahmad.; TT Dang.; H Reinke.; P Langer. Regioselective Suzuki cross-coupling reactions of 2, 3, 4, 5-tetrabromo-1-methylpyrrole. Tetrahedron Letters. 200849 (10), 1698-1700.
JR Carson.; DN McKinstry.; S Wong. 5-Benzoyl-1-methylpyrrole-2-acetic acids as antiinflammatory agents. J. Med. Chem. 197114 (7), 646-647.
Lithiation occurs at the 2-position. Excess n-BuLi in the presence of TMEDA leads to 2,5-dimetallation: J. Chem. Soc. Perkin I, 887 (1977).
Reaction of benzenoid aromatics with lactones under Friedel-Crafts conditions normally results in alkylation. With 1-methylpyrrole and - or δ-lactones in the presence of AlCl3, acylation at the 2-position predominates: Tetrahedron Lett., 36, 6739 (1995).
Hazard Statements: H225-H302-H315-H335
Highly flammable liquid and vapour. Harmful if swallowed. Causes skin irritation. May cause respiratory irritation.
Precautionary Statements: P260-P201-P280a-P304+P340-P405-P501a
Do not breathe dust/fume/gas/mist/vapours/spray. Obtain special instructions before use. Wear protective gloves and eye/face protection. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.