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
Empirical Formula (Hill Notation):
C6H9N
CAS Number:
Molecular Weight:
95.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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Reactions of the Perfluoroalkylnitriles. VIII. Syntheses of 1, 3, 5-Triazines with Specific Groups in the 2, 4, or 6 Positions.
Brown H, et al.
The Journal of Organic Chemistry, 32(1), 231-233 (1967)
The structure of pyrrole salts and the basic strengths of some simple pyrroles.
Bullock, E.
Canadian Journal of Chemistry, 36(12), 1686-1690 (1958)
Lavinia A Trifoi et al.
Frontiers in chemistry, 8, 470-470 (2020-06-26)
Molecules that respond to input stimulations to produce detectable outputs can be exploited to mimic Boolean logic operators and reproduce basic arithmetic functions. We have designed a two-state fluorescent probe with tunable emission wavelength for the construction of a molecular
Prodigiosene [5-(2-pyrryl)-2, 21-dipyrrylmethene] and some substituted prodigiosenes.
Hearn WR, et al.
The Journal of Organic Chemistry, 35(1), 8376-8382 (1970)
Kepeng Lei et al.
Talanta, 170, 314-321 (2017-05-16)
The sensitive and selective fluorescence probe for hydroxyl radical analysis is of significance because hydroxyl radical plays key roles in many physiological and pathological processes. In this work, a novel organic fluorescence molecular probe OHP for hydroxyl radical is synthesized
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