| Identification | More | [Name]
4-Iodoimidazole | [CAS]
71759-89-2 | [Synonyms]
1H-IMIDAZOLE, 4-IODO-
4(5)-IODO-1(H)-IMIDAZOLE
4(5)-IODOIMIDAZOLE
4-IODO-1H-IMIDAZOLE
4-IODOIMIDAZOLE
AKOS 91347
4-lodoimidazole | [EINECS(EC#)]
676-945-3 | [Molecular Formula]
C3H3IN2 | [MDL Number]
MFCD01632213 | [Molecular Weight]
193.97 | [MOL File]
71759-89-2.mol |
| Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
137-138°C | [Boiling point ]
348.5±15.0 °C(Predicted) | [density ]
2.335±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [solubility ]
Methanol (Slightly) | [form ]
Solid | [pka]
11.46±0.10(Predicted) | [color ]
White to Pale Yellow | [Sensitive ]
Light Sensitive | [Usage]
Imidazole rings are found in numberous natural compounds such as enzymes, nucleic acid, and alkaloids that play a role in biological processes | [BRN ]
1616 | [InChI]
InChI=1S/C3H3IN2/c4-3-1-5-2-6-3/h1-2H,(H,5,6) | [InChIKey]
BHCMXJKPZOPRNN-UHFFFAOYSA-N | [SMILES]
C1NC(I)=CN=1 | [CAS DataBase Reference]
71759-89-2(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Imidazole rings are found in numberous natural compounds such as enzymes, nucleic acid, and alkaloids that play a role in biological processes | [Uses]
suzuki reaction | [Synthesis]
4-Iodoimidazole is a chemical compound that is used in the synthesis of other compounds. It can be synthesized by cross-coupling reactions with 4-iodoaniline and 4-bromoimidazole. | [References]
[1] Patent: US2012/245144, 2012, A1. Location in patent: Page/Page column 118
[2] Journal of Medicinal Chemistry, 1996, vol. 39, # 15, p. 3001 - 3013
[3] Patent: WO2006/38100, 2006, A1. Location in patent: Page/Page column 78 |
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