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81945-73-5 | 1H-Pyrazol-1-ol
CAS No: 81945-73-5 Catalog No: AG0055VS MDL No:MFCD11850516
Product Description
Catalog Number:
AG0055VS
Chemical Name:
1H-Pyrazol-1-ol
CAS Number:
81945-73-5
Molecular Formula:
C3H4N2O
Molecular Weight:
84.0767
MDL Number:
MFCD11850516
IUPAC Name:
1-hydroxypyrazole
InChI:
InChI=1S/C3H4N2O/c6-5-3-1-2-4-5/h1-3,6H
InChI Key:
QVCIPIYWPSPRFA-UHFFFAOYSA-N
SMILES:
On1cccn1
EC Number:
279-854-3
Properties
Complexity:
48.1
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
84.032g/mol
Formal Charge:
0
Heavy Atom Count:
6
Hydrogen Bond Acceptor Count:
2
Hydrogen Bond Donor Count:
1
Isotope Atom Count:
0
Molecular Weight:
84.078g/mol
Monoisotopic Mass:
84.032g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
38A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.3
Literature
| Title | Journal |
|---|---|
| Novel 4-(piperidin-4-yl)-1-hydroxypyrazoles as gamma-aminobutyric acid(A) receptor ligands: synthesis, pharmacology, and structure-activity relationships. | Journal of medicinal chemistry 20100422 |
| Hydration of diazoles in water solution: pyrazole. A theoretical and X-ray diffraction study. | Physical chemistry chemical physics : PCCP 20091107 |
| N-Hydroxypyrazolyl glycine derivatives as selective N-methyl-D-aspartic acid receptor ligands. | Journal of medicinal chemistry 20080724 |
| Novel 5-substituted 1-pyrazolol analogues of ibotenic acid: synthesis and pharmacology at glutamate receptors. | Bioorganic & medicinal chemistry 20070515 |
| The respective N-hydroxypyrazole analogues of the classical glutamate receptor ligands ibotenic acid and (RS)-2-amino-2-(3-hydroxy-5-methyl-4-isoxazolyl)acetic acid. | European journal of pharmacology 20040919 |
| N-Alkoxypyrazoles as biomimetics for the alkoxyphenyl group in tamoxifen. | Bioorganic & medicinal chemistry 20030417 |
| Novel 1-hydroxyazole bioisosteres of glutamic acid. Synthesis, protolytic properties, and pharmacology. | Journal of medicinal chemistry 20020103 |
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