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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:
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

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

Signal Word

Warning

Hazard 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

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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The synthesis of Knorr's pyrrole by inverse addition.
Cooney JV, et al.
Organic preparations and procedures international, 15(4), 292-295 (1983)
Synthesis and spectral properties of new boron dipyrromethene dyes.
Binchen G, et al.
Dyes and Pigments, 73(2), 206-210 (2007)
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
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)
The structure of pyrrole salts and the basic strengths of some simple pyrroles.
Bullock, E.
Canadian Journal of Chemistry, 36(12), 1686-1690 (1958)

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