131709
Pyrrole
reagent grade, 98%
Synonym(s):
Azole, Divinylenimine, Imidole
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About This Item
Empirical Formula (Hill Notation):
C4H5N
CAS Number:
Molecular Weight:
67.09
Beilstein:
1159
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39151603
PubChem Substance ID:
NACRES:
NA.22
form:
liquid
Assay:
98%
Recommended Products
grade
reagent grade
Quality Level
vapor density
2.31 (vs air)
Assay
98%
form
liquid
refractive index
n20/D 1.508 (lit.)
bp
131 °C (lit.)
mp
−23 °C (lit.)
density
0.967 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
c1cc[nH]c1
InChI
1S/C4H5N/c1-2-4-5-3-1/h1-5H
InChI key
KAESVJOAVNADME-UHFFFAOYSA-N
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General description
Pyrrole is a heterocyclic aromatic compound that can undergo electrophilic aromatic substitution.
Application
Pyrrole was used in the electropolymerisation of macroporous conducting polymer films. It was also used to study the hydrogen-bond mediated coupling of 1,2,3-triazole to pyrrole.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
96.8 °F - closed cup
Flash Point(C)
36 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Pyrrole
Chen MZ and Tsai AS
eEROS (Encyclopedia of Reagents for Organic Synthesis), 1-4 (2001)
Guillaume Lautrette et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(6), 1547-1553 (2014-01-10)
Starting from a previously described aromatic oligoamide helically folded capsule that binds tartaric acid with high affinity and diastereoselectivity, we demonstrate the feasibility of the direct in situ modification of the helix backbone, which results in a conformational change that
Electrochemical syntheses of highly ordered macroporous conducting polymers grown around self-assembled colloidal templates.
Bartlett PN, et al.
Journal of Materials Chemistry, 11(3), 849-853 (2001)
Jian Wen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(4), 974-978 (2014-01-01)
Hydrogen-bond mediated coupling of 1,2,3-triazoles to indoles and pyrroles results in N2 selective functionalization of the triazole moiety in moderate to excellent yields. The reaction was tolerant of un-, mono- and disubstituted triazoles and was applied to synthesize tryptophan derived
Woo Young Hong et al.
Biomaterials, 35(36), 9573-9580 (2014-09-07)
Here, we propose an integrated multifunctional system constructed by conductive disulfide-biotin-doped polypyrrole nanowires (SS-biotin-Ppy NWs) for capture, release, and in situ quantification of circulating tumor cells (CTCs). A well-ordered three-dimensional nanowire structure equipped with a monoclonal antibody offers a significant
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