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2-Amino-5-fluoropyridine

Names

[ CAS No. ]:
21717-96-4

[ Name ]:
2-Amino-5-fluoropyridine

[Synonym ]:
2-Pyridinamine, 5-fluoro-
5-Fluorpyridin-2-amin
MFCD01861120
5-Fluoro-2-pyridinamine
5-fluoropyridin-2-amine
5-fluoro-2-aminepyridine
2-Amino-5-fluoropyridine
2-Amino-5-fluoroypyridine
5-FLUORO-2-AMINOPYRIDINE

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
195.1±20.0 °C at 760 mmHg

[ Melting Point ]:
93-97 °C(lit.)

[ Molecular Formula ]:
C5H5FN2

[ Molecular Weight ]:
112.105

[ Flash Point ]:
71.8±21.8 °C

[ Exact Mass ]:
112.043678

[ PSA ]:
38.91000

[ LogP ]:
0.82

[ Vapour Pressure ]:
0.4±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.554

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
UN2811

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ HS Code ]:
2933399090

Precursor & DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Discovery of 2-[5-(4-Fluorophenylcarbamoyl)pyridin-2-ylsulfanylmethyl]phenylboronic Acid (SX-517): Noncompetitive Boronic Acid Antagonist of CXCR1 and CXCR2.

J. Med. Chem. 57(20) , 8378-97, (2014)

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 ...

Tandem approach for the synthesis of imidazo [1, 2-a] pyridines from alcohols. Ramesha AB, et al.

Tetrahedron Lett. 54(1) , 95-100, (2013)

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)


More Articles


Related Compounds