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822-55-9 | (1H-Imidazol-4-yl)methanol
CAS No: 822-55-9 Catalog No: AG0055ZO MDL No:MFCD00266718
Product Description
Catalog Number:
AG0055ZO
Chemical Name:
(1H-Imidazol-4-yl)methanol
CAS Number:
822-55-9
Molecular Formula:
C4H6N2O
Molecular Weight:
98.1032
MDL Number:
MFCD00266718
IUPAC Name:
1H-imidazol-5-ylmethanol
InChI:
InChI=1S/C4H6N2O/c7-2-4-1-5-3-6-4/h1,3,7H,2H2,(H,5,6)
InChI Key:
QDYTUZCWBJRHKK-UHFFFAOYSA-N
SMILES:
OCc1c[nH]cn1
UNII:
QD0132T507
Properties
Complexity:
57.7
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
98.048g/mol
Formal Charge:
0
Heavy Atom Count:
7
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
2
Isotope Atom Count:
0
Molecular Weight:
98.105g/mol
Monoisotopic Mass:
98.048g/mol
Rotatable Bond Count:
1
Topological Polar Surface Area:
48.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.8
Literature
| Title | Journal |
|---|---|
| Conformationally constrained histidines in the design of peptidomimetics: strategies for the χ-space control. | International journal of molecular sciences 20110101 |
| Effects of 4-methylimidazole on cerebral glutamate decarboxylase activity and specific GABA receptor binding in mice. | Toxicology mechanisms and methods 20090301 |
| Two isomorphous ZnII/CoII complexes with tri-tert-butoxysilanethiol and histamine, and (4-hydroxymethyl-1H-imidazole-kappaN)bis(tri-tert-butoxysilanethiolato-kappa2O,S)zinc(II). | Acta crystallographica. Section C, Crystal structure communications 20080701 |
| Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. | The Journal of biological chemistry 20020419 |
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