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P73609

Sigma-Aldrich

Pyrrole-2-carboxylic acid

99%

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Synonym(s):
2-Mialine, 2-Minaline
Empirical Formula (Hill Notation):
C5H5NO2
CAS Number:
Molecular Weight:
111.10
Beilstein/REAXYS Number:
80825
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

powder

mp

204-208 °C (dec.) (lit.)

SMILES string

OC(=O)c1ccc[nH]1

InChI

1S/C5H5NO2/c7-5(8)4-2-1-3-6-4/h1-3,6H,(H,7,8)

InChI key

WRHZVMBBRYBTKZ-UHFFFAOYSA-N

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This Item
C95803134198150134
Pyrrole-2-carboxylic acid 99%

P73609

Pyrrole-2-carboxylic acid

Cyclobutane-1,1-dicarboxylic acid 99%

C95803

Cyclobutane-1,1-dicarboxylic acid

Isoquinoline-1-carboxylic acid 99%

150134

Isoquinoline-1-carboxylic acid

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100

form

powder

form

crystals

form

-

form

-

mp

204-208 °C (dec.) (lit.)

mp

158 °C (lit.)

mp

192-194 °C (lit.)

mp

164 °C (dec.) (lit.)

Application

Employed in the synthesis of cholecystokinin antagonists, benzopyran antihypertensives, and azepinediones.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Customers Also Viewed

V A Ashwood et al.
Journal of medicinal chemistry, 33(9), 2667-2672 (1990-09-01)
The synthesis and antihypertensive activity of a series of novel 4-(substituted-carbonylamino)-2H-1-benzopyran-3-ols, administered orally to conscious spontaneously hypertensive rats, are described. Optimum activity was observed for compounds with alkyl, amino, or aryl groups flanking the carbonyl group. Of the alkyl and
Giulia Moro et al.
Bioelectrochemistry (Amsterdam, Netherlands), 134, 107540-107540 (2020-05-04)
The immobilization of biomolecules at screen printed electrodes for biosensing applications is still an open challenge. To enrich the toolbox of bioelectrochemists, graphite screen printed electrodes (G-SPE) were modified with an electropolymerized film of pyrrole-2-carboxilic acid (Py-2-COOH), a pyrrole derivative
Michał Kizling et al.
Nanomaterials (Basel, Switzerland), 10(8) (2020-08-09)
A significant problem still exists with the low power output and durability of the bioelectrochemical fuel cells. We constructed a fuel cell with an enzymatic cascade at the anode for efficient energy conversion. The construction involved fabrication of the flow-through
J F Kerwin et al.
Journal of medicinal chemistry, 34(12), 3350-3359 (1991-12-11)
The intriguing structural similarities of glutamic acid based cholecystokinin (CCK) antagonists (A-64718 and A-65186) and the benzodiazepine CCK antagonist MK-329 (L-364,718) have been reported. Efforts to include the weak CCK antagonist benzotript into this construct utilizing a similar approach have
Australian Journal of Chemistry, 43, 355-355 (1990)

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