(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol
CAS: 187970-01-0
Molecular Formula: C8H7N3O2
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol - Names and Identifiers
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol - Physico-chemical Properties
| Molecular Formula | C8H7N3O2 |
| Molar Mass | 177.16 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD12027001 |
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol - Risk and Safety
| Hazard Class | IRRITANT |
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol - Introduction
(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol is an organic compound with the molecular formula C8H7N3O2. It is a white solid, soluble in organic solvents such as chloroform and ethanol.
One of the main uses of (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol is as an intermediate in organic synthesis. It can be used to synthesize biologically active compounds, such as antibacterial drugs, anticancer drugs, etc. In addition, it can also be used for the preparation of coordination compounds, heterocyclic compounds, heterocyclic metal complexes, and the like.
A method for preparing a (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol can be obtained by reacting a (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanamine with formaldehyde in the presence of hydrochloric acid. Specific synthetic steps need of course to be carried out in the laboratory using specific conditions.
Regarding safety information, since no specific literature or experimental data is provided, accurate safety information cannot be provided. However, like most organic compounds, appropriate safety measures should be taken when using and handling (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol, such as wearing gloves, goggles and Use ventilation outside the laboratory. Before using any chemical substance, its nature should be understood in advance and used in accordance with the correct method and laboratory safety regulations. If necessary, reference should be made to the relevant safety data sheet and the MSDS (Material Safety Data Sheet) of the chemical. It should be emphasized that the practical application of the use and preparation method is best carried out in a professional laboratory environment and in accordance with relevant laws and regulations.
One of the main uses of (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol is as an intermediate in organic synthesis. It can be used to synthesize biologically active compounds, such as antibacterial drugs, anticancer drugs, etc. In addition, it can also be used for the preparation of coordination compounds, heterocyclic compounds, heterocyclic metal complexes, and the like.
A method for preparing a (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol can be obtained by reacting a (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanamine with formaldehyde in the presence of hydrochloric acid. Specific synthetic steps need of course to be carried out in the laboratory using specific conditions.
Regarding safety information, since no specific literature or experimental data is provided, accurate safety information cannot be provided. However, like most organic compounds, appropriate safety measures should be taken when using and handling (3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol, such as wearing gloves, goggles and Use ventilation outside the laboratory. Before using any chemical substance, its nature should be understood in advance and used in accordance with the correct method and laboratory safety regulations. If necessary, reference should be made to the relevant safety data sheet and the MSDS (Material Safety Data Sheet) of the chemical. It should be emphasized that the practical application of the use and preparation method is best carried out in a professional laboratory environment and in accordance with relevant laws and regulations.
Last Update：2024-04-09 21:32:52
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(3-Pyridin-2-yl-1,2,4-oxadiazol-5-yl)methanol
126583-37-7
2-Aminobenzothiazole
Glycyrrhizinic acid, potassium salt
2-(2-Chloropropanoyl)-3-(difluoromethyl)benzonitrile
Fomesafen sodium
Ethanol, 2,2'-[[4-cyclopropyl-6-(cyclopropylamino)-1,3,5-triazin-2-yl]imino]bis- (9CI)
21-(6-thioxo-3,6-dihydro-9H-purin-9-yl)pregn-4-ene-3,20-dione
Methanamine, N-(1-phenylpropylidene)-
L-Serine, O-[O-(N-acetyl-4,7,8,9-tetra-O-acetyl-1-methyl-β-neuraminosyl)-(2→6)-O-[2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1→3)]-4-O-acetyl-2-(acetylamino)-2-deoxy-α-D-galactopyranosyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- (9CI)
126583-37-7
2-Aminobenzothiazole
Glycyrrhizinic acid, potassium salt
2-(2-Chloropropanoyl)-3-(difluoromethyl)benzonitrile
Fomesafen sodium
Ethanol, 2,2'-[[4-cyclopropyl-6-(cyclopropylamino)-1,3,5-triazin-2-yl]imino]bis- (9CI)
21-(6-thioxo-3,6-dihydro-9H-purin-9-yl)pregn-4-ene-3,20-dione
Methanamine, N-(1-phenylpropylidene)-
L-Serine, O-[O-(N-acetyl-4,7,8,9-tetra-O-acetyl-1-methyl-β-neuraminosyl)-(2→6)-O-[2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1→3)]-4-O-acetyl-2-(acetylamino)-2-deoxy-α-D-galactopyranosyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- (9CI)