All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C5H5FN2
CAS Number:
Molecular Weight:
112.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
mp
93-97 °C (lit.)
SMILES string
Nc1ccc(F)cn1
InChI
1S/C5H5FN2/c6-4-1-2-5(7)8-3-4/h1-3H,(H2,7,8)
InChI key
YJTXQLYMECWULH-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Russell J Needham et al.
Journal of inorganic biochemistry, 210, 111154-111154 (2020-08-11)
Twenty-four novel organometallic osmium(II) phenylazopyridine (AZPY) complexes have been synthesised and characterised; [Os(η6-arene)(5-RO-AZPY)X]Y, where arene = p-cym or bip, AZPY is functionalized with an alkoxyl (O-R, R = Me, Et, nPr, iPr, nBu) or glycolic (O-{CH2CH2O}nR*, n = 1-4, R* = H, Me, or Et) substituent on the
Dean Y Maeda et al.
Journal of medicinal chemistry, 57(20), 8378-8397 (2014-09-26)
The G protein-coupled chemokine receptors CXCR1 and CXCR2 play key roles in inflammatory diseases and carcinogenesis. In inflammation, they activate and recruit polymorphonuclear cells (PMNs) through binding of the chemokines CXCL1 (CXCR1) and CXCL8 (CXCR1 and CXCR2). Structure-activity studies that
Tandem approach for the synthesis of imidazo [1, 2-a] pyridines from alcohols.
Ramesha AB, et al.
Tetrahedron Letters, 54(1), 95-100 (2013)
Synthesis of 2-Amino-5-Fluoropyridine.
MA ZP, et al.
Journal of Chemical Engineering of Chinese Universities / Gao Xiao Hua Xue Gong Cheng Xue Bao, 4, 015-015 (2008)
Syntheses of 2-chloro-and 2-amino-5-fluoropyridines and isolation of a novel difluoroboryl imidate.
Smakula Hand E and Baker DC.
Synthesis, 12, 905-908 (1989)
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