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
로그인조직 및 계약 가격 보기
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
분석
97%
형태
powder
mp
94-96 °C (lit.)
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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관련 카테고리
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
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
The ITQ-37 mesoporous chiral zeolite.
Sun J, et al.
Nature, 458(7242), 1154-1154 (2009)
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)
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
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)
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)
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