595934
2,3-二溴-N-甲基马来酰亚胺
99%
别名:
1-Methyl-3,4-dibromomaleimide, 3,4-Dibromo-1-methyl-1H-pyrrole-2,5-dione, 3,4-Dibromo-1-methyl-2,5-dihydropyrrole-2,5-dione, 3,4-Dibromo-1-methylpyrrole-2,5-dione, 3,4-Dibromo-N-methylmaleimide, 3,4-Dibromo-N-methylpyrrole-2,5-dione, N-Methyl-2,3-dibromomaleimide, N-Methyldibromomaleimide
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关于此项目
经验公式（希尔记法）:
C5H3Br2NO2
化学文摘社编号:
分子量:
268.89
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
2,3-二溴-N-甲基马来酰亚胺, 99%
InChI
1S/C5H3Br2NO2/c1-8-4(9)2(6)3(7)5(8)10/h1H3
SMILES string
CN1C(=O)C(Br)=C(Br)C1=O
InChI key
CKITYUQKOJMMOI-UHFFFAOYSA-N
assay
99%
mp
120-124 °C (lit.)
functional group
bromo
imide
maleimide
Quality Level
Application
2,3-Dibromo-N-methylmaleimide can be used to synthesize bis-indolylmaleimides via reaction with indolyl magnesium bromide. It can also undergo mono-cross coupling with triorganoindium derivatives which can be further coupled with naphthodithiophene to form an intermediate for [5]thiahelicene synthesis.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
"Metal-catalyzed cross-coupling reactions of halomaleic anhydrides and halomaleimides: synthesis of structurally interesting and biologically important natural and unnatural products"
Deore SP and Argade PN
Synthesis, 46(03), 281-289 (2014)
Synthesis of arcyriarubin B and related bisindolylmaleimides.
Brenner M, et al.
Tetrahedron, 44(10), 2887-2892 (1988)
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