557781
N-苄基-2,3-二溴马来酰亚胺
97%
别名:
1-苄基-3,4-二溴-吡咯-2,5-二酮
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关于此项目
经验公式（希尔记法）:
C11H7Br2NO2
化学文摘社编号:
分子量:
344.99
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
产品名称
N-苄基-2,3-二溴马来酰亚胺, 97%
InChI
1S/C11H7Br2NO2/c12-8-9(13)11(16)14(10(8)15)6-7-4-2-1-3-5-7/h1-5H,6H2
SMILES string
BrC1=C(Br)C(=O)N(Cc2ccccc2)C1=O
InChI key
DZYLZHRCCNTQCS-UHFFFAOYSA-N
assay
97%
form
solid
mp
117-120 °C (lit.)
functional group
bromo
imide
maleimide
phenyl
Application
N-Benzyl-2,3-dibromomaleimide may be used in the synthesis of the following maleimide-based dyes, which can be employed in fluorescence quenching:
- 2,3-bis(3-indolyl)-N-benzylmaleimide
- 2,3-bis(2′-methyl-3-indolyl)-N-benzylmaleimide
- 2,3-bis(2-pyrrolyl)-N-benzylmaleimide
- 2-aryl-N-benzyl-3-bromomaleimides via suzuki cross coupling reaction with aryl boronic acid
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
法规信息
新产品
此项目有
Bifunctional maleimide dyes as selective anion sensors.
Lin Z, et al.
Tetrahedron, 65(27), 5216-5221 (2009)
"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)
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