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390836

Sigma-Aldrich

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:
625-82-1
Molecular Weight:
95.14
EC Number:
210-912-2
MDL number:
MFCD00192088
UNSPSC Code:
12352100
PubChem Substance ID:
24864348
NACRES:
NA.22

Quality Level

200

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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315 - H319 - H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Photolysis of 2, 5-and 2, 4-dimethylpyrrole vapors at room temperature.
Wu EC and Heicklen J.
Canadian Journal of Chemistry, 50(11), 1678-1689 (1972)
Addition of pyrroles to 1, 4-benzoquinone.
Bullock, E.
Canadian Journal of Chemistry, 36(12), 1744-1744 (1958)
Seda Çetindere et al.
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.
Lifshitz A, et al.
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.
Brown H, et al.
The Journal of Organic Chemistry, 32(1), 231-233 (1967)
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