5-Brom-3-nitropyridin-2-amin

Names

[ Name ]:
5-Brom-3-nitropyridin-2-amin

[Synonym ]:
2-Pyridinamine,5-bromo-3-nitro
5-bromo-3-nitro-pyridin-2-ylamine
MFCD00047441
5-Bromo-3-Nitro-2-Pyridinamine
5-Brom-3-nitropyridin-2-amin
5-bromo-3-nitropyridin-2-amine
2-Amino-5-bromo-3-nitropyridine
2-Pyridinamine, 5-bromo-3-nitro-
3-nitro-5-bromopyridin-2-amine
2-Amino-3-nitro-5-bromopyridine

Biological Activity

[Description]:

2-Amino-5-bromo-3-nitropyridine 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]:
1.9±0.1 g/cm3

[ Boiling Point ]:
302.9±37.0 °C at 760 mmHg

[ Melting Point ]:
205-208 °C(lit.)

[ Molecular Formula ]:
C₅H₄BrN₃O₂

[ Molecular Weight ]:
218.01

[ Flash Point ]:
137.0±26.5 °C

[ Exact Mass ]:
216.948685

[ PSA ]:
84.73000

[ LogP ]:
2.79

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.683

MSDS

Click to get detail 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 ]:
Xn:Harmful

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S37/39-S36/37/39-S22

[ 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

Discovery of 6-({4-[2-(4-tert-butylphenyl)-1H-benzimidazol-4-yl]piperazin-1-yl}methyl)quinoxaline (WAY-207024): an orally active antagonist of the gonadotropin releasing hormone receptor (GnRH-R).

J. Med. Chem. 52(7) , 2148-52, (2009)

A potent, highly insoluble, GnRH antagonist with a 2-phenyl-4-piperazinylbenzimidazole template and a quinoxaline-2,3-dione pharmacophore was modified to maintain GnRH antagonist activity and improve ...

2, 3-Diaminopyridine. Fox BA and Threlfall TL.

Organic Synth. , 34-34, (1973)