1,2-DIMETHYL-4-NITRO-1H-IMIDAZOLE

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Names

[ CAS No. ]:
13230-04-1

[ Name ]:
1,2-DIMETHYL-4-NITRO-1H-IMIDAZOLE

[Synonym ]:
1,2-Dimethyl-4-nitro-1H-imidazole
1,2-Dimethyl-4-nitroimidazol
1,2-dimethyl-4-nitro-imidazole
Imidazole,1,2-dimethyl-4-nitro
1,2-Dimethyl-4-nitro-1H-imidazol
dimethyl-1,2 nitro-4 imidazole
EINECS 236-201-7

Chemical & Physical Properties

[ Density]:
1.36g/cm3

[ Boiling Point ]:
313.7ºC at 760mmHg

[ Melting Point ]:
179-182ºC

[ Molecular Formula ]:
C5H7N3O2

[ Molecular Weight ]:
141.12800

[ Flash Point ]:
143.5ºC

[ Exact Mass ]:
141.05400

[ PSA ]:
63.64000

[ LogP ]:
1.15990

[ Vapour Pressure ]:
0.000901mmHg at 25°C

[ Index of Refraction ]:
1.598

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
NI4925000
CHEMICAL NAME :
Imidazole, 1,2-dimethyl-4-nitro-
CAS REGISTRY NUMBER :
13230-04-1
BEILSTEIN REFERENCE NO. :
0121504
LAST UPDATED :
199612
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C5-H7-N3-O2
MOLECULAR WEIGHT :
141.15
WISWESSER LINE NOTATION :
T5N CNJ A1 B1 DNW

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Mutation in microorganisms
TEST SYSTEM :
Bacteria - Klebsiella pneumoniae
DOSE/DURATION :
5 mmol/L/20H
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 66,207,1979

Safety Information

[ HS Code ]:
2933290090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 2-Methyl-4-nitroimidazole
  • methyl iodide
  • Dimethyl Carbonate
  • Metronidazole
  • 1,2-Dimethylimidazole
  • Dimethyl sulfate

DownStream

Customs

[ HS Code ]: 2933290090

[ Summary ]:
2933290090. other compounds containing an unfused imidazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Related Compounds

  • 5-Bromo-1,2-dimethyl-4-nitro-1H-imidazole
  • 5-chloro-1,2-dimethyl-4-nitro-1h-imidazole
  • 5-methoxy-1,2-dimethyl-4-nitro-1h-imidazole
  • 1,2-DIMETHYL-4-NITRO-1H-IMIDAZOLE-5-CARBOXYLIC ACID
  • N,N-Bis(2-chloroethyl)-1,2-dimethyl-4-nitro-1H-imidazole-5-carboxamide
  • N-(4-(Bis(2-chloroethyl)amino)phenyl)-1,2-dimethyl-4-nitro-1H-imidazole-5-carboxamide
  • 2,2-Dimethyl-octahydrocyclopenta[e][1,3]oxazine
  • 2-(4-((3,4-dimethylphenyl)sulfonyl)piperazin-1-yl)-N-ethyl-6-methylpyrimidin-4-amine
  • 1-(3-Methylsulfanylpropanoyl)pyrrolidine-2-carboxylic acid
  • 4-(Benzo[d][1,3]dioxol-5-yl)butan-1-ol
  • 2-[2-(4-Cyanophenyl)ethoxy]ethanol
  • N-ethyl-2-(4-((4-methoxyphenyl)sulfonyl)piperazin-1-yl)-6-methylpyrimidin-4-amine
  • 2-(4-((4-ethoxyphenyl)sulfonyl)piperazin-1-yl)-N-ethyl-6-methylpyrimidin-4-amine
  • 3-Pyrimidinecarboxylic acid, 6-(4-(dimethylamino)phenyl)-1-ethyl-1,4-dihydro-4-oxo-
  • Beta,beta-Dichloro-alpha-(trifluoromethyl)styrene
  • N-(5-tetrazolyl)-4-nitro-2-pyridinecarboxamide
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