Key Documents

View All Documentation

P27100

N-Phenylmaleimide

Name: <I>N</I>-Phenylmaleimide
Brand: ALDRICH

97%

Synonym(s):

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

Select a Size

Change View

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

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

Quality Level

200

assay

97%

form

solid

bp

162-163 °C/12 mmHg (lit.)

mp

85-87 °C (lit.)

SMILES string

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

InChI key

HIDBROSJWZYGSZ-UHFFFAOYSA-N

Description

pictograms

GHS06,GHS09

signalword

Danger

hcodes

H301,H400

pcodes

P264 - P273 - P301 + P310 - P391 - P405 - P501

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Adaptive variable-weighted support vector machine as optimized by particle swarm optimization algorithm with application of QSAR studies.

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

N-phenylmaleimide derivatives as mimetic agents of the pro-inflammatory process: myeloperoxidase activation.

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)

Diastereo- and enantioselective [3 + 2] cycloaddition reaction of Morita-Baylis-Hillman carbonates of isatins with N-phenylmaleimide catalyzed by Me-DuPhos.

Yan Wang et al.

The Journal of organic chemistry, 77(8), 4143-4147 (2012-04-05)

A Me-DuPhos-catalyzed efficient asymmetric [3 + 2] cycloaddition reaction between Morita-Baylis-Hillman carbonates of isatins and N-phenylmaleimide has been developed. This reaction constructs three chiral centers in one step to afford spirocyclopentaneoxindoles in good yields (up to 84%) with excellent diastereo-

View All Related Papers