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Merck

131709

Pyrrole

reagent grade, 98%

Synonym(s):

Azole, Divinylenimine, Imidole

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About This Item

Empirical Formula (Hill Notation):
C4H5N
CAS Number:
109-97-7
Molecular Weight:
67.09
NACRES:
NA.22
PubChem Substance ID:
24848030
eCl@ss:
39151603
UNSPSC Code:
12352100
EC Number:
203-724-7
MDL number:
MFCD00005216
Beilstein/REAXYS Number:
1159

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Product Name

Pyrrole, reagent grade, 98%

InChI key

KAESVJOAVNADME-UHFFFAOYSA-N

InChI

1S/C4H5N/c1-2-4-5-3-1/h1-5H

SMILES string

c1cc[nH]c1

grade

reagent grade

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

Quality Level

200

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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.

General description

Pyrrole is a heterocyclic aromatic compound that can undergo electrophilic aromatic substitution.

signalword

Danger

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB3407
STBL0361
STBK3502
STBK3185
STBJ8211

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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
Pyrrole
Chen MZ and Tsai AS
eEROS (Encyclopedia of Reagents for Organic Synthesis), 1-4 (2001)
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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