160865
2-Acetyl-1-methylpyrrole
98%
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About This Item
Empirical Formula (Hill Notation):
C7H9NO
CAS Number:
Molecular Weight:
123.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
213-247-6
MDL number:
Product Name
2-Acetyl-1-methylpyrrole, 98%
InChI key
NZFLWVDXYUGFAV-UHFFFAOYSA-N
InChI
1S/C7H9NO/c1-6(9)7-4-3-5-8(7)2/h3-5H,1-2H3
SMILES string
CC(=O)c1cccn1C
assay
98%
form
liquid
refractive index
n20/D 1.542 (lit.)
bp
200-202 °C (lit.)
density
1.04 g/mL at 25 °C (lit.)
functional group
ketone
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Application
2-Acetyl-1-methylpyrrole was employed as model pyrrole to investigate the antioxidative activity of nonenzymatic browning reactions. It was employed as catalyst for the sulfonylation of spectinomycin.
General description
Reduction of 2-acetyl-1-methylpyrrole with sodium borohydride has been investigated.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
154.4 °F - closed cup
flash_point_c
68 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Francisco J Hidalgo et al.
Journal of agricultural and food chemistry, 51(19), 5703-5708 (2003-09-04)
The present investigation was undertaken to study how the antioxidative activity (AA) of nonenzymatic browning reactions is changing at the same time that the browning (by the pyrrole polymerization mechanism) is being produced. The antioxidative activities of eight model pyrroles
F J Hidalgo et al.
The Journal of biological chemistry, 268(22), 16190-16197 (1993-08-05)
The reaction of (E)-4,5-epoxy-(E)-2-heptenal with butylamine and glycine methyl ester produced brown macromolecular pigments, which showed fluorescent characteristics similar to lipofuscins. This polymerization reaction implies in the first step the formation of 1-alkyl-2-(1'-hydroxyalkyl)pyrroles (IV, VI). Compounds IV and VI have
K Tsuji et al.
Journal of chromatography, 333(2), 365-380 (1985-10-04)
A normal-phase high-performance liquid chromatographic (HPLC) method has been developed for the assay of spectinomycin hydrochloride and spectinomycin sulfate for detection at 254 nm. The method involves pre-column derivatization of secondary amines of spectinomycin with 2-naphthalenesulfonyl chloride (NSCl) using a
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