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
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)
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
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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