추천 제품
Quality Level
분석
97%
mp
76-80 °C (lit.)
작용기
bromo
fluoro
nitrile
SMILES string
Fc1ccc(Br)cc1C#N
InChI
1S/C7H3BrFN/c8-6-1-2-7(9)5(3-6)4-10/h1-3H
InChI key
GYCNHFWRPJXTSB-UHFFFAOYSA-N
애플리케이션
5-Bromo-2-fluorobenzonitrile may be used for the preparation of the following compounds:
- (E)-5-(2-cyclopropylvinyl)-2-fluorobenzonitrile and methyl-3-amino-5-bromobenzo[b]thiophene-2-carboxylate
- (S)-[2-[5-(3-cyano-4-fluoro-phenyl)-pyridin-3-yloxy]-1-(1H-indol-3-ylmethyl)-ethyl]-carbamic acid tert-butyl ester
- 4-fluoro-3-cyano-3′-tributyltinbenzhydrol
- 4-fluoro-3-cyano-3′-iodobenzhydrol
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
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, Faceshields, Gloves
Microwave-assisted synthesis of 3-aminobenzo [b] thiophene scaffolds for the preparation of kinase inhibitors.
Organic & Biomolecular Chemistry (2015)
Bioconjugate chemistry, 14(2), 287-294 (2003-03-20)
The synthesis of a benzophenone-based labeling compound designed for comparative imaging studies with both in vivo positron emission tomograph (PET) and single-photon computed tomography (SPECT) and ex vivo autoradiography is described. The new compound can be labeled with either F-18
Bioorganic & medicinal chemistry, 14(20), 6832-6846 (2006-07-18)
A series of heteroaryl-pyridine containing inhibitors of Akt are reported. The synthesis and structure-activity relationships are discussed, leading to the discovery of a indazole-pyridine analogue (K(i)=0.16 nM). These compounds bind in the ATP binding site, are potent, ATP competitive, and
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