6-Bromo-3H-purin-2-amine

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Names

[ CAS No. ]:
82499-03-4

[ Name ]:
6-Bromo-3H-purin-2-amine

[Synonym ]:
9H-purin-2-amine, 6-bromo-
MFCD01321309
6-Bromo-3H-purin-2-amine
7H-Purin-2-amine, 6-bromo-
Purine, 2-amino-6-bromo-
1H-Purin-2-amine, 6-bromo-
6-bromo-9H-purin-2-amine
6-bromo-7H-purin-2-amine

Chemical & Physical Properties

[ Density]:
2.1±0.1 g/cm3

[ Boiling Point ]:
642.5±58.0 °C at 760 mmHg

[ Melting Point ]:
>350ºC

[ Molecular Formula ]:
C5H4BrN5

[ Molecular Weight ]:
214.023

[ Flash Point ]:
342.4±32.3 °C

[ Exact Mass ]:
212.964996

[ PSA ]:
80.48000

[ LogP ]:
0.10

[ Vapour Pressure ]:
0.0±1.9 mmHg at 25°C

[ Index of Refraction ]:
1.851

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Guanine

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Arxula adeninivorans recombinant adenine deaminase and its application in the production of food with low purine content.

J. Appl. Microbiol. 115(5) , 1134-46, (2013)

Construction of a transgenic Arxula adeninivorans strain that produces a high concentration of adenine deaminase and investigation into the application of the enzyme in the production of food with low...

Synthesis of Some Biologically Active Halogenopurines. Hu YL, et al.

J. Korean Chem. Soc. 54(4) , 429-436, (2010)

Theoretical studies on the interaction of guanine riboswitch with guanine and its closest analogues. Ling B, et al.

Mol. Simul. 36(12) , 929-938, (2010)


More Articles

Related Compounds

  • 6-Morpholin-4-yl-9H-purin-2-ylamine
  • 6-((4-(Aminomethyl)benzyl)oxy)-7H-purin-2-amine
  • 6-O-Methylguanine
  • O6-Benzylguanine
  • Purine, 2-amino-6-methyl-8-phenyl- (8CI)
  • 629-25-4 (Hydrochloride salt)
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 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
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide
  • N-[3-(Aminooxy)propyl]-N-butyl-1-butanamine