Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
BrC6H3(F)CN
CAS Number:
Molecular Weight:
200.01
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
5-Bromo-2-fluorobenzonitrile, 97%
InChI
1S/C7H3BrFN/c8-6-1-2-7(9)5(3-6)4-10/h1-3H
SMILES string
Fc1ccc(Br)cc1C#N
InChI key
GYCNHFWRPJXTSB-UHFFFAOYSA-N
assay
97%
mp
76-80 °C (lit.)
functional group
bromo
fluoro
nitrile
Quality Level
Application
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
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Microwave-assisted synthesis of 3-aminobenzo [b] thiophene scaffolds for the preparation of kinase inhibitors.
Bagley MC, et al.
Organic & Biomolecular Chemistry (2015)
Zizhong Li et al.
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
Keith W Woods et al.
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
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