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Merck

P27100

N-Phenylmaleimide

97%

Synonym(s):

1-Phenyl-pyrrole-2,5-dione, 1-[4-(Acetoxy)phenyl]maleimide

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About This Item

Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
941-69-5
Molecular Weight:
173.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24898352
EC Number:
213-382-0
Beilstein/REAXYS Number:
125098
MDL number:
MFCD00005502
Assay:
97%
Form:
solid

Key Documents

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InChI key

HIDBROSJWZYGSZ-UHFFFAOYSA-N

InChI

1S/C10H7NO2/c12-9-6-7-10(13)11(9)8-4-2-1-3-5-8/h1-7H

SMILES string

O=C1C=CC(=O)N1c2ccccc2

assay

97%

form

solid

bp

162-163 °C/12 mmHg (lit.)

mp

85-87 °C (lit.)

Quality Level

200

Related Categories

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

hcodes

H301,H400

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

Substances Subject to be Indicated Names

ishl_indicated

Substances Subject to be Notified Names

ishl_notified

P27100-25G: + P27100-VAR: + P27100-100G: + P27100-1KG: + P27100-BULK:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH0000
BCCC4131
BCCC0414
BCBV0645
BCBS6819V

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Vânia F Noldin et al.
Pharmacological reports : PR, 63(3), 772-780 (2011-08-23)
Myeloperoxidase (MPO) is an important enzyme that catalyzes the reaction between hydrogen peroxide and chloride to generate hypochlorous acid, which oxidizes a range of biomolecules and has been associated with inflammatory diseases. The synthetic compounds N-phenylmaleimide (NFM) and 4-methyl-N-phenylmaleimide (Me-NFM)
Masato Hoshino et al.
Chemical & pharmaceutical bulletin, 56(4), 480-484 (2008-04-02)
Diels-Alder reactions between N-phenylmaleimide, acting as the dienophile, and 2(1H)-pyridones having a methoxy or a chloro substituent, were carried out, under atmospheric and high pressure conditions, to give the corresponding isoquinuclidine derivatives. Stereoselectivity of the Diels-Alder reactions was studied using
Nicolas Matuszak et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 45(3), 263-271 (2011-12-01)
The endocannabinoid system is implicated in numerous physiopathological processes while more and more pieces of evidence wave the link between this complex machinery and cancer related phenomenon. In these lines, we confirmed the effects of 2-arachidonoylglycerol (2-AG), the main endocannabinoid
L Xie et al.
Biochemistry, 38(18), 5925-5931 (1999-05-08)
Alkylation of myosin's Cys-707 (SH1) and Cys-697 (SH2) has profound consequences for myosin's ability to interact with actin and hydrolyze MgATP. Pre-steady-state measurements of myosin-S1 alkylated at SH1 and SH2 by N-phenylmaleimide (NPM) in the presence of ATP were taken
Jian-Hui Wen et al.
Talanta, 84(1), 13-18 (2011-02-15)
Representing a compound by a numerous structural descriptors becomes common in quantitative structure-activity relationship (QSAR) studies. As every descriptor carries molecular structure information more or less, it seems more advisable to investigate all the possible descriptor vectors rather than traditional
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