5-Bromopyridin-2-ol

Names

[ Name ]:
5-Bromopyridin-2-ol

[Synonym ]:
5-Bromo-2-pyridone
3-Bromo-6-hydroxypyridine
5-bromopyridin-2-ol
5-bromo-1H-pyrid-2-one
5-Bromo-2(1H)-pyridinone
2(1H)-Pyridinone, 5-bromo-
5-bromo-1H-pyridine-2-one
MFCD00234042
5-bromopyridin-2-one
5-Bromo-2-pyridinol
5-Bromo-2-hydroxypyridine
5-Bromopyridin-2(1H)-one
5-Bromo-2-hydroxypyrdine

Biological Activity

[Description]:

5-Bromopyridin-2-ol is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
322.8±22.0 °C at 760 mmHg

[ Melting Point ]:
180-183 °C(lit.)

[ Molecular Formula ]:
C₅H₄BrNO

[ Molecular Weight ]:
174.00

[ Flash Point ]:
149.0±22.3 °C

[ Exact Mass ]:
172.947617

[ PSA ]:
33.12000

[ LogP ]:
0.62

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.614

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H315-H319-H335

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

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

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

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

Facile one-pot synthesis of N-difluoromethyl-2-pyridone derivatives.

Org. Lett. 8(17) , 3805-8, (2006)

[reaction: see text] A novel one-pot synthesis of N-difluoromethyl-2-pyridones is described. N-(Pyridin-2-yl)acetamide derivatives were excellent precursors for the preparation of N-difluoromethyl-2-p...