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

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Names

[ CAS No. ]:
7033-39-8

[ 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)


More Articles

Related Compounds

  • 6-Amino-5-bromo-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
  • 5-CHLORO-1,3-DIMETHYLPYRIMIDINE-2,4(1H,3H)-DIONE
  • 5-bromo-1,3,6-trimethylpyrimidine-2,4(1H,3H)-dione
  • 5-benzoyl-6-(bromomethyl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
  • 5-((2R,5R)-5-(hydroxymethyl)-4-oxotetrahydrofuran-2-yl)-1,3-dimethylpyrimidine-2,4(1H,3H)-dione
  • 6-(CHLOROMETHYL)-1,3-DIMETHYLPYRIMIDINE-2,4(1H,3H)-DIONE
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 3-(8-Bromo-2,3-dihydro-1,4-benzodioxin-6-yl)-2-hydroxypropanoic acid
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 3-[(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-(methylsulfanyl)butanamido]-2,2-difluoropropanoic acid