5-Bromo-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

Names

[ Name ]:
5-Bromo-1,3-dimethylpyrimidine-2,4(1H,3H)-dione

[Synonym ]:
5-bromo-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
MFCD00191846
T6NVNVJ A1 C1 EE
5-bromo-1,3-dimethylpyrimidine-2,4-dione
1,3-Dimethyl-5-bromouracil
5-bromo-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
5-Bromo-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione
Uracil, 5-bromo-1,3-dimethyl-
2,4(1H,3H)-Pyrimidinedione, 5-bromo-1,3-dimethyl-

Chemical & Physical Properties

[ Density]:
1.7±0.1 g/cm3

[ Boiling Point ]:
242.1±50.0 °C at 760 mmHg

[ Melting Point ]:
182-185ºC(lit.)

[ Molecular Formula ]:
C₆H₇BrN₂O₂

[ Molecular Weight ]:
219.036

[ Flash Point ]:
100.2±30.1 °C

[ Exact Mass ]:
217.969086

[ PSA ]:
44.00000

[ LogP ]:
0.75

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.585

[ Storage condition ]:
2-8°C

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

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933599090

Synthetic Route

Click to get detail synthetic route

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

Excited state structures and decay dynamics of 1,3-dimethyluracils in solutions: resonance Raman and quantum mechanical calculation study.

J. Phys. Chem. B 117(39) , 11660-9, (2013)

The resonance Raman spectroscopic study of the excited state structural dynamics of 1,3-dimethyluracil (DMU), 5-bromo-1,3-dimethyluracil (5BrDMU), uracil, and thymine in water and acetonitrile were re...

Photochemical coupling of 5-bromo-1,3-dimethyluracil and its 6-alkyl derivatives to 3-methylindole and N alpha-acetyl-L-tryptophan methyl ester.

J. Photochem. Photobiol. B, Biol. 3(4) , 565-74, (1989)

Photochemical reactions between 5-bromo-1,3-dimethyluracils and 3-substituted indoles in acetone solution were studied. Irradiation (lambda greater than 290 nm) of 5-bromo-1,3-dimethyluracil (1) and N...

Photoinduced cross-coupling reaction of 5-bromo-1, 3-dimethyluracil to electron-rich aromatics. Ito S, et al.

Tetrahedron 37(1) , 45-50, (1981)