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Merck
CN

N20204

4-Nitrophenylacetic acid

ReagentPlus®, 99%

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About This Item

Linear Formula:
O2NC6H4CH2CO2H
CAS Number:
Molecular Weight:
181.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-168-5
Beilstein/REAXYS Number:
1911801
MDL number:
Assay:
99%
Form:
powder
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InChI

1S/C8H7NO4/c10-8(11)5-6-1-3-7(4-2-6)9(12)13/h1-4H,5H2,(H,10,11)

InChI key

YBADLXQNJCMBKR-UHFFFAOYSA-N

SMILES string

OC(=O)Cc1ccc(cc1)[N+]([O-])=O

product line

ReagentPlus®

assay

99%

form

powder

Quality Level

Related Categories

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

CorrosionEnvironment

signalword

Danger

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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L Baltzer et al.
Bioorganic & medicinal chemistry, 7(1), 83-91 (1999-04-13)
Four-helix bundle proteins have been designed that catalyze the hydrolysis and transesterification reactions of p-nitrophenyl esters by a cooperative nucleophilic and general acid mechanism. The catalysts consist of two 42-residue peptides that fold into helix-loop-helix motifs and dimerise. They have
Halis T Balaydın et al.
European journal of medicinal chemistry, 54, 423-428 (2012-06-13)
A series of bisphenol, bromophenol, and methoxyphenol derivatives (2-24) including the natural bromophenols vidalol B, 3,4,6-tribromo-5-(2,5-dibromo-3,4-dihydroxybenzyl)benzene-1,2-diol (2) and 5,5'-methylenebis(3,4,6-tribromo-benzene-1,2-diol) (3) were prepared. In the current study, inhibition of four human carbonic anhydrase (hCA, EC 4.2.1.1) isozymes, I, II, IV, and
Mingxing Xie et al.
Drug metabolism and disposition: the biological fate of chemicals, 30(5), 541-547 (2002-04-16)
Carboxylesterases hydrolyze numerous endogenous and foreign compounds with diverse structures. Humans and rodents express multiple forms of carboxylesterases, which share a high degree of sequence identity (approximately 70%). Alignment analyses locate in carboxylesterases several functional subsites such the catalytic triad
Roselyne Castonguay et al.
Bioorganic & medicinal chemistry, 10(12), 4185-4191 (2002-11-05)
The enzyme gamma-glutamyl transpeptidase (GGT), implicated in many physiological processes, catalyses the transfer of a gamma-glutamyl from a donor substrate to an acyl acceptor substrate, usually an amino acid or a peptide. In order to investigate which moieties of the
Teruko Imai et al.
Drug metabolism and disposition: the biological fate of chemicals, 33(8), 1185-1190 (2005-05-24)
The absorption characteristics of temocapril were investigated using Caco-2 cells, and the esterases expressed in Caco-2 cells were identified. Temocapril was almost completely hydrolyzed to temocaprilat during transport across Caco-2 cells. Hydrolysis experiments of temocapril in Caco-2 cell 9000g supernatant

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