5-Bromopyrimidine

Names

[ Name ]:
5-Bromopyrimidine

[Synonym ]:
5-BroMopyriMidine 25GR
5-bromopyrimdine
5-Bromopyrimidine
5-BROMOISATINIC ANHYDRIDE
PYRIMIDINE,2-BROMO
MFCD00014601
Pyrimidine, 5-bromo-
5-pyrimidyl bromide
5-bromo-pyrimidine
5-bromo-pyrimidin
5-BROMOPYRIMIDINE 0.98
5-BROMOPYRIMIDINE MIN
EINECS 224-992-1
5-bromopyridine
bromopyrimidine
PYRIMIDINE,5-BROMO

Biological Activity

[Description]:

5-Bromopyrimidine 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

[In Vitro]

5-Bromopyrimidine 用于通过钯催化的有氧和无配体铃木反应合成 N-杂芳基取代的 9-芳基咔唑基衍生物。

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
201.4±13.0 °C at 760 mmHg

[ Melting Point ]:
69 °C

[ Molecular Formula ]:
C₄H₃BrN₂

[ Molecular Weight ]:
158.98

[ Flash Point ]:
75.6±19.8 °C

[ Exact Mass ]:
157.947952

[ PSA ]:
25.78000

[ LogP ]:
0.66

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

[ Index of Refraction ]:
1.568

[ Storage condition ]:
Keep Cold

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 ]:
Xi:Irritant

[ Risk Phrases ]:
R36/38

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

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933599090

[ Summary ]:
2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

A highly efficient and aerobic protocol for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives via a palladium-catalyzed ligand-free Suzuki reaction.

Org. Biomol. Chem. 10(39) , 7875-83, (2012)

A palladium-catalyzed aerobic and ligand-free Suzuki reaction in aqueous ethanol has been developed for the synthesis of N-heteroaryl substituted 9-arylcarbazolyl derivatives. A number of N-heteroaryl...

The new NHS: restricting GPs' access to x ray services.

BMJ 302(6791) , 1541, (1991)

Efficient nucleophilic substitution reactions of pyrimidyl and pyrazyl halides with nucleophiles under focused microwave irradiation. Cherng,Y-J.

Tetrahedron 58(5) , 887-90, (2002)