390836
2,4-Dimethylpyrrole
97%
Synonym(s):
2,4-Dimethyl-1-pyrrole, 2,4-Dimethyl-1H-pyrrole, 2,4-Dimethyl-3H-pyrrole
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About This Item
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.496 (lit.)
bp
165-167 °C (lit.)
density
0.924 g/mL at 25 °C (lit.)
SMILES string
Cc1c[nH]c(C)c1
InChI
1S/C6H9N/c1-5-3-6(2)7-4-5/h3-4,7H,1-2H3
InChI key
MFFMQGGZCLEMCI-UHFFFAOYSA-N
Related Categories
General description
2,4-Dimethylpyrrole is a substituted pyrrole. Its synthesis by using ethyl acetoacetate as starting material has been reported. Its basicity has been evaluated from UV spectral data. Its photodecomposition on irradiation has been reported to afford H2, CH4, C2H6 and polymeric products.
Application
2,4-Dimethylpyrrole may be used in the synthesis of the following:
- 2,5-bis(2′,4′-dimethyl-5′-pyrryl)p-benzoquinone
- boron dipyrromethene (BODIPY) dyes
- 2,4-dimethyl-6-methoxyprodigiosene
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Photolysis of 2, 5-and 2, 4-dimethylpyrrole vapors at room temperature.
Canadian Journal of Chemistry, 50(11), 1678-1689 (1972)
Addition of pyrroles to 1, 4-benzoquinone.
Canadian Journal of Chemistry, 36(12), 1744-1744 (1958)
Journal of fluorescence, 29(5), 1143-1152 (2019-08-14)
In the present work, novel water-soluble cyclotriphosphazene derivatives (3b and 4b) were synthesized by 'click' reactions between cyclotriphosphazene derivative with hydrophilic glycol side groups (2) and Bodipy's (3a and 4a). All newly synthesized compounds (2, 3b and 4b) were characterized
Thermal decomposition and ring expansion in 2, 4-dimethylpyrrole. Single pulse shock tube and modeling studies.
The Journal of Physical Chemistry A, 107(24), 4851-4861 (2003)
Reactions of the Perfluoroalkylnitriles. VIII. Syntheses of 1, 3, 5-Triazines with Specific Groups in the 2, 4, or 6 Positions.
The Journal of Organic Chemistry, 32(1), 231-233 (1967)
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