100919
N-(4-Bromobutyl)phthalimide
98%
동의어(들):
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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모든 사진(1)
About This Item
실험식(Hill 표기법):
C12H12BrNO2
CAS Number:
Molecular Weight:
282.13
Beilstein:
164119
EC Number:
MDL number:
UNSPSC 코드:
12352111
PubChem Substance ID:
NACRES:
NA.22
추천 제품
분석
98%
반응 적합성
reagent type: cross-linking reagent
reagent type: linker
mp
76-80 °C (lit.)
작용기
bromo
폴리머 구조
functionality: heterobifunctional
SMILES string
O=C1N(CCCCBr)C(C2=CC=CC=C21)=O
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
InChI key
UXFWTIGUWHJKDD-UHFFFAOYSA-N
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애플리케이션
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
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)
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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