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Home > Imidazoles > 16093-82-6
16093-82-6 | 1H-Imidazol-2-carboxamide
CAS No: 16093-82-6 Catalog No: AG001VIP MDL No:MFCD09261275
Product Description
Catalog Number:
AG001VIP
Chemical Name:
1H-Imidazol-2-carboxamide
CAS Number:
16093-82-6
Molecular Formula:
C4H5N3O
Molecular Weight:
111.1020
MDL Number:
MFCD09261275
IUPAC Name:
1H-imidazole-2-carboxamide
InChI:
InChI=1S/C4H5N3O/c5-3(8)4-6-1-2-7-4/h1-2H,(H2,5,8)(H,6,7)
InChI Key:
NMIZONYLXCOHEF-UHFFFAOYSA-N
SMILES:
NC(=O)c1ncc[nH]1
Properties
Complexity:
104
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
111.043g/mol
Formal Charge:
0
Heavy Atom Count:
8
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
111.104g/mol
Monoisotopic Mass:
111.043g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
71.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.7
Literature
| Title | Journal |
|---|---|
| Unsymmetrical tetrasubstituted ureas from tertiary carbamoylimidazole: activation by AlMe3. | Organic & biomolecular chemistry 20120821 |
| Synthesis, physicochemical properties, and hydrogen bonding of 4(5)-substituted 1-H-imidazole-2-carboxamide, a potential universal reader for DNA sequencing by recognition tunneling. | Chemistry (Weinheim an der Bergstrasse, Germany) 20120507 |
| Photoinduced intramolecular tryptophan oxidation and excited-state behavior of [Re(L-AA)(CO)3(α-diimine)](+) (L = pyridine or imidazole, AA = tryptophan, tyrosine, phenylalanine). | Inorganic chemistry 20110704 |
| Organogels based on 1H-imidazolecarboxamide amphiphiles. | Langmuir : the ACS journal of surfaces and colloids 20090804 |
| Parallel synthesis of an imidazole-4,5-dicarboxamide library bearing amino acid esters and alkanamines. | Molecules (Basel, Switzerland) 20081215 |
| Optimization of imidazole amide derivatives as cannabinoid-1 receptor antagonists for the treatment of obesity. | Bioorganic & medicinal chemistry letters 20070515 |
| Non-hormonal systemic therapy in men with hormone-refractory prostate cancer and metastases: a systematic review from the Cancer Care Ontario Program in Evidence-based Care's Genitourinary Cancer Disease Site Group. | BMC cancer 20060101 |
| Demonstration of an alternative mechanism for G-to-G cross-link formation. | Journal of the American Chemical Society 20050126 |
| Malignant melanoma--future prospects. | Acta dermatovenerologica Croatica : ADC 20050101 |
| A new approach for syntheses of 2',3'-dideoxy-2',3'-dehydronucleosides using 2,2-difluoro-1,3-dimethylimidazolidine (DFI) as a dehydrating reagent. | Nucleosides, nucleotides & nucleic acids 20030101 |
| A facile synthesis of [N1,NH(2-)(15)N(2)], [N3,NH(2-)(15)N(2)] and [N2, N3,NH(2-)(15)N(3)]-labeled adenine. | The Journal of organic chemistry 20010921 |
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