389412
N-Methylmaleimide
97%
동의어(들):
1-Methyl-1H-pyrrole-2,5-dione, 1-Methyl-2,5-dihydro-1H-pyrrole-2,5-dione, 1-Methylpyrrole-2,5-dione, N-Methyl maleic imide, N-Methylpyrrole-2,5-dione
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모든 사진(2)
About This Item
실험식(Hill 표기법):
C5H5NO2
CAS Number:
Molecular Weight:
111.10
Beilstein:
108550
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
97%
양식
powder
mp
94-96 °C (lit.)
작용기
imide
maleimide
SMILES string
CN1C(=O)C=CC1=O
InChI
1S/C5H5NO2/c1-6-4(7)2-3-5(6)8/h2-3H,1H3
InChI key
SEEYREPSKCQBBF-UHFFFAOYSA-N
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애플리케이션
N-Methylmaleimide can be used:
- In the synthesis of organic structure directing agents for designing silicogermanate zeolites.
- As a dienophile in Diels-Alder reaction.
- For the synthesis of biologically active pyrrolo[2,1-a]isoquinolines.
- As a dipolarophile in [3 + 2] dipolar addition reactions.
- As a co-monomer in atom transfer radical polymerization of styrene to obtain styrene copolymers with programmed microstructure.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Oral - Skin Corr. 1B - Skin Sens. 1
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Visible-light-induced oxidation/[3+ 2] cycloaddition/oxidative aromatization sequence: a photocatalytic strategy to construct pyrrolo [2, 1-a] isoquinolines.
Zou YQ, et al.
Angewandte Chemie (International Edition in English), 50(31), 7171-7175 (2011)
A facile procedure for controlling monomer sequence distribution in radical chain polymerizations.
Pfeifer S and Lutz JF
Journal of the American Chemical Society, 129(31), 9542-9543 (2007)
Asymmetric organocatalytic three-component 1, 3-dipolar cycloaddition: Control of stereochemistry via a chiral br?nsted acid activated dipole.
Chen XH, et al.
Journal of the American Chemical Society, 130(17), 5652-5653 (2008)
Eun Jo Du et al.
PLoS genetics, 12(1), e1005773-e1005773 (2016-01-05)
Pathogen expulsion from the gut is an important defense strategy against infection, but little is known about how interaction between the intestinal microbiome and host immunity modulates defecation. In Drosophila melanogaster, dual oxidase (Duox) kills pathogenic microbes by generating the
Hui Zhou et al.
The Analyst, 143(10), 2390-2396 (2018-04-27)
Glutathione (GSH) exhibits many cellular functions in human pathologies. A sensitive and simple method capable of assaying GSH would be useful to understand the mechanism of GSH-related diseases. In this study, a new colorimetric and fluorescent off-on probe, 3-oxo-3H-phenoxazin-7-ylthiophene-2-carboxylate, is
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