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
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39151603
UNSPSC Code:
12352100
EC Number:
203-724-7
MDL number:
Beilstein/REAXYS Number:
1159
Assay:
98%
Form:
liquid
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
96.8 °F - closed cup
flash_point_c
36 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Articles
From Form to Function: Molding Porous Materials in Three Dimensions by Colloidal Crystal Templating
Related Content
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
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
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 131709-100ML | 04061838252005 |
| 131709-2.5L | 04061838230379 |
| 131709-25ML | 04061838252012 |
| 131709-500ML | 04061838252029 |