ethyl 5-methyl-4-imidazolecarboxylate

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Names

[ CAS No. ]:
51605-32-4

[ Name ]:
ethyl 5-methyl-4-imidazolecarboxylate

[Synonym ]:
Ethyl 4-methyl-1H-imidazole-5-carboxylate
EINECS 257-315-3
ETHYL 5-METHYL-1H-IMIDAZOLE-4-CARBOXYLATE
1H-imidazole-4-carboxylic acid, 5-methyl-, ethyl ester
ethyl 5-methyl-4-imidazolecarboxylate
Ethyl 4-methyl-5-imidazolecarboxylate
1H-Imidazole-5-carboxylic acid, 4-methyl-, ethyl ester
MFCD00014487
1H-imidazole-5-carboxylic acid, 4-methyl-,ethyl ester

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
323.7±22.0 °C at 760 mmHg

[ Melting Point ]:
204-206ºC(lit.)

[ Molecular Formula ]:
C7H10N2O2

[ Molecular Weight ]:
154.167

[ Flash Point ]:
149.5±22.3 °C

[ Exact Mass ]:
154.074234

[ PSA ]:
54.98000

[ LogP ]:
1.05

[ Vapour Pressure ]:
0.0±0.7 mmHg at 25°C

[ Index of Refraction ]:
1.520

MSDS

Click to get detail MSDS

Safety Information

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933290090

Synthetic Route

Click to get detail synthetic route

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%

Articles

Cobalt(II) coordination compounds of ethyl 4-methyl-5-imidazolecarboxylate: chemical and biochemical characterization on photosynthesis and seed germination.

Bioinorg. Chem. Appl. , 93-108, (2005)

In this work we present the synthesis, structural and spectroscopic characterization of Co(2+) coordination compounds with ethyl 4-methyl-5-imidazolecarboxylate (emizco). The effects of emizco, the me...


More Articles

Related Compounds

  • ethyl 5-methyl-4-imidazolecarboxylate
  • ETHYL 5-METHYL-4-([3-(TRIFLUOROMETHYL)ANILINO]CARBONYL)-3-ISOXAZOLECARBOXYLATE
  • ethyl 5-methyl-4-oxo-1-phenyl-1,2,4,5-tetrahydro-3H-pyridazino[4,5-b]indole-3-carboxylate
  • ethyl 5-methyl-4-phenylthiazole-2-carboxylate
  • ethyl 5-methyl-4-methylidenehex-2-ynoate
  • ethyl 5-methyl-4-piperidin-1-ylpyridine-3-carboxylate