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P27100

Sigma-Aldrich

N-Phenylmaleimide

97%

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C10H7NO2
Número CAS:
941-69-5
Peso molecular:
173.17
Beilstein:
125098
Número CE:
213-382-0
Número MDL:
MFCD00005502
Código UNSPSC:
12352100
ID de substância PubChem:
24898352
NACRES:
NA.22

Ensaio

97%

Formulário

solid

p.e.

162-163 °C/12 mmHg (lit.)

pf

85-87 °C (lit.)

cadeia de caracteres SMILES

O=C1C=CC(=O)N1c2ccccc2

InChI

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

chave InChI

HIDBROSJWZYGSZ-UHFFFAOYSA-N

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Pictogramas

Skull and crossbonesEnvironment
GHS06,GHS09

Palavra indicadora

Danger

Frases de perigo

H301,H400

Classificações de perigo

Acute Tox. 3 Oral - Aquatic Acute 1

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCH0000
BCCC4131
BCCC0414
BCBV0645
BCBS6819V

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Nickel(II) chloride hexahydrate puriss. p.a., ≥98%

Sigma-Aldrich

31462

Nickel(II) chloride hexahydrate

Furan ≥99%

Sigma-Aldrich

185922

Furan

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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