Recommended Products
Assay
97%
form
solid
mp
117-120 °C (lit.)
SMILES string
BrC1=C(Br)C(=O)N(Cc2ccccc2)C1=O
InChI
1S/C11H7Br2NO2/c12-8-9(13)11(16)14(10(8)15)6-7-4-2-1-3-5-7/h1-5H,6H2
InChI key
DZYLZHRCCNTQCS-UHFFFAOYSA-N
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B - Skin Sens. 1
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
"Metal-catalyzed cross-coupling reactions of halomaleic anhydrides and halomaleimides: synthesis of structurally interesting and biologically important natural and unnatural products"
Synthesis, 46(03), 281-289 (2014)
Bifunctional maleimide dyes as selective anion sensors.
Tetrahedron, 65(27), 5216-5221 (2009)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service