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About This Item
Linear Formula:
FC6H3(CN)NO2
CAS Number:
Molecular Weight:
166.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
97%
mp
76-80 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(F)c(c1)C#N
InChI
1S/C7H3FN2O2/c8-7-2-1-6(10(11)12)3-5(7)4-9/h1-3H
InChI key
YLACBMHBZVYOAP-UHFFFAOYSA-N
General description
2-Fluoro-5-nitrobenzonitrile can be prepared from 2-fluorobenzonitrile via nitration.
Application
2-Fluoro-5-nitrobenzonitrile may be used in the preparation of:
- 2-fluoro-5-aminobenzonitrile
- ethyl 3-amino-5-nitro-benzo[b]thiophene-2-carboxylate
- 1-methyl-5-nitro-1H-indazol-3-ylamine
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Certificates of Analysis (COA)
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Synthesis, antiproliferative activity, and in silico insights of new 3-benzoylamino-benzo [b] thiophene derivatives.
Martorana A, et al.
European Journal of Medicinal Chemistry, 90, 537-546 (2015)
Mimi L Quan et al.
Journal of medicinal chemistry, 48(6), 1729-1744 (2005-03-18)
Modification of a series of pyrazole factor Xa inhibitors to incorporate an aminobenzisoxazole as the P(1) ligand resulted in compounds with improved selectivity for factor Xa relative to trypsin and plasma kallikrein. Further optimization of the P(4) moiety led to
A method for the regioselective synthesis of 1-alkyl-1H-indazoles.
Liu HJ, et al.
Tetrahedron, 69(19), 3907-3912 (2013)
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