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1-Methylpyrrole, 99%
1-Methylpyrrole, 99%
1-Methylpyrrole, 99%
Thermo Scientific Chemicals

1-Methylpyrrole, 99%

CAS: 96-54-8 | C5H7N | 81.118 g/mol
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Catalog number B21451.AP
also known as B21451-AP
Price (EUR)
233,00
Each
Quantity:
500 mL
Request bulk or custom format
Price (EUR)
233,00
Each
Chemical Identifiers
CAS96-54-8
IUPAC Name1-methyl-1H-pyrrole
Molecular FormulaC5H7N
InChI KeyOXHNLMTVIGZXSG-UHFFFAOYSA-N
SMILESCN1C=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow to brown
Refractive Index1.4855-1.4885 @ 20?C
FormLiquid
Assay (GC)≥98.5%
1-Methylpyrrole, can be used as organic synthetic materials, widely used in medicine. It is also used as a pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1-Methylpyrrole, can be used as organic synthetic materials, widely used in medicine. It is also used as a pharmaceutical intermediate.

Solubility
Soluble in organic solvents such as alcohol and so on, but insoluble in water.

Notes
Keep away from acids, acid chlorides, acid anhydrides, strong oxidizing agents, carbon dioxide. Keep away from acids, acid chlorides, acid anhydrides, strong oxidizing agents, carbon dioxide. Stable under normal temperatures and pressures.
RUO – Research Use Only

General References:

  1. 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.
  2. JR Carson.; DN McKinstry.; S Wong. 5-Benzoyl-1-methylpyrrole-2-acetic acids as antiinflammatory agents. J. Med. Chem. 197114 (7), 646-647.
  3. 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).
  4. 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).