100919
N-(4-溴丁基)邻苯二甲酰亚胺
98%
别名:
1-Phthalimido-4-bromobutane, 2-(4-Bromobutyl)-2,3-dihydro-1H-isoindole-1,3-dione, 2-(4-Bromobutyl)phthalimide, 4-Bromobutylphthalimide
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关于此项目
经验公式（希尔记法）:
C12H12BrNO2
化学文摘社编号:
分子量:
282.13
UNSPSC Code:
12352111
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-401-2
Beilstein/REAXYS Number:
164119
MDL number:
产品名称
N-(4-溴丁基)邻苯二甲酰亚胺, 98%
InChI key
UXFWTIGUWHJKDD-UHFFFAOYSA-N
InChI
1S/C12H12BrNO2/c13-7-3-4-8-14-11(15)9-5-1-2-6-10(9)12(14)16/h1-2,5-6H,3-4,7-8H2
SMILES string
O=C1N(CCCCBr)C(C2=CC=CC=C21)=O
assay
98%
reaction suitability
reagent type: cross-linking reagent
reagent type: linker
mp
76-80 °C (lit.)
functional group
bromo
polymer architecture
functionality: heterobifunctional
Quality Level
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Application
N-(4-Bromobutyl)phthalimide can be used to synthesize:
- Biologically important N4,N9-disubstituted 4,9-diaminoacridine derivatives.
- Imidazo[4,5-b]pyridine derivatives applicable in the preparation of ketolide antibiotics.
- Calix[4]arene and thiacalix[4]arene-based oxamate ligands.
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
法规信息
新产品
此项目有
Zhanhui Wang et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 971, 10-13 (2014-09-28)
The application of antibodies to small molecules in the field of bioanalytics requires antibodies with stable biological activity and high purity; thus, there is a growing interest in developing rapid, inexpensive and effective procedures to obtain such antibodies. In this
Synthesis of multivalent oxamate ligands based on calix [4] arene and thiacalix [4] arene backbones in 1, 3-Alternate conformation
Noamane MH, et al.
Tetrahedron, 73, 4259-4264 (2017)
Development of a synthetic route towards N4, N9-disubstituted 4, 9-diaminoacridines: On the way to multi-stage antimalarials
Fonte M, et al.
Tetrahedron Letters, 60, 1166-1169 (2019)
Synthesis of derivatives of imidazo [4,5-b] pyridine: Novel sulfur contained side chains for macrolide antibiotics
Liu L, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 19, 1-4 (2008)
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