产品名称
2,3-二溴马来酰亚胺, 97%
InChI
1S/C4HBr2NO2/c5-1-2(6)4(9)7-3(1)8/h(H,7,8,9)
SMILES string
BrC1=C(Br)C(=O)NC1=O
InChI key
BIKSKRPHKQWJCW-UHFFFAOYSA-N
assay
97%
form
solid
mp
228-231 °C (lit.)
functional group
bromo
maleimide
Quality Level
Application
2,3-二溴马来酰亚胺可用于以下合成:
- 四氢呋喃中的2-溴-3-(1-H-吲哚-3-基)马来酰亚胺与吲哚基溴化镁的反应
- 2-二溴-3-丙基硫磺酸马来取代与丙硫醇和乙酸钠在甲醇中的反应
General description
2,3-二溴马来酰亚胺是一种环状酰亚胺,基于从头计算和密度泛函理论(DFT)计算得出的偶极矩为0.30德拜。
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B - Skin Sens. 1
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
A method for preparing water soluble cyclic polymers
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This Review aims to highlight key aspects of tetrapyrrole-based antibody-drug conjugates (ADCs) and significant developments in the field since 2010. Many new conjugation methods have been developed and employed in the past decade, and associated with this, there has been
Strong fluorescence enhancement of 2-bromo-3-(1H-indol-3-yl) maleimide upon coordination to a Lewis-acidic metal complex.
Kaletas BK, et al.
Chemical Communications (Cambridge, England), 7, 776-777 (2002)
Polarizability and first-order hyperpolarizability of cyclic imides.
Asghari-Khiavi M, et al.
Journal of Molecular Structure: THEOCHEM, 910(1), 56-60 (2009)
Ting Bai et al.
Macromolecular bioscience, 20(7), e1900438-e1900438 (2020-05-15)
Targeting the distinct cholesterol metabolism of tumor cells is proposed as a novel way to treat tumors. Blocking acyl-CoA cholesterol acyltransferase-1 (ACAT-1) by the inhibitor avasimible (Ava), which elevates intracellular free cholesterol levels, is shown to effectively induce apoptosis. However
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