AKOS PAO-1264
3-(3-Methyl-4-nitro-1H-pyrazol-1-yl)propanoic acid
CAS: 956396-51-3
Molecular Formula: C7H9N3O4
AKOS PAO-1264 - Names and Identifiers
AKOS PAO-1264 - Physico-chemical Properties
| Molecular Formula | C7H9N3O4 |
| Molar Mass | 199.16 |
| Sensitive | IRRITANT |
| MDL | MFCD03419614 |
AKOS PAO-1264 - Introduction
propanoic acid is an organic compound, also referred to as MNP. Its molecular formula is C8H10N4O4.
Nature:
-Appearance: Colorless crystalline solid
-Melting point: 156-158°C
-Solubility: Soluble in common organic solvents such as alcohols, ketones, esters and ethers
-Stability: stable to light and heat, not easy to decompose
Use:
-MNPs are commonly used as reagents and intermediates in organic synthesis
-It can be used to synthesize other organic compounds, such as drugs and dyes
-In the medical field, MNPs may have antibacterial and anti-inflammatory activities, so they may be used to design new drug molecules
Preparation Method:
- 3-(propanoic) p-acid can be synthesized by a variety of methods, the most common is by the reaction of 3-methyl -1-acetone and 4-nitro-3-methylpyrazole.
Safety Information:
-Specific toxicity and hazard data for MNPs have not been publicly reported, so safety measures such as wearing protective gloves and glasses should be taken when handling MNPs in a well-ventilated laboratory environment. When using MNP, the relevant chemical safety practices should be followed.
Nature:
-Appearance: Colorless crystalline solid
-Melting point: 156-158°C
-Solubility: Soluble in common organic solvents such as alcohols, ketones, esters and ethers
-Stability: stable to light and heat, not easy to decompose
Use:
-MNPs are commonly used as reagents and intermediates in organic synthesis
-It can be used to synthesize other organic compounds, such as drugs and dyes
-In the medical field, MNPs may have antibacterial and anti-inflammatory activities, so they may be used to design new drug molecules
Preparation Method:
- 3-(propanoic) p-acid can be synthesized by a variety of methods, the most common is by the reaction of 3-methyl -1-acetone and 4-nitro-3-methylpyrazole.
Safety Information:
-Specific toxicity and hazard data for MNPs have not been publicly reported, so safety measures such as wearing protective gloves and glasses should be taken when handling MNPs in a well-ventilated laboratory environment. When using MNP, the relevant chemical safety practices should be followed.
Last Update：2024-04-09 19:06:00
