2-(aminomethyl)-5-phenyl-3-furoic acid hydrochloride
2-Aminomethyl-5-phenyl-furan-3-carboxylic acid
CAS: 695191-66-3
Molecular Formula: C12H11NO3
2-(aminomethyl)-5-phenyl-3-furoic acid hydrochloride - Names and Identifiers
2-(aminomethyl)-5-phenyl-3-furoic acid hydrochloride - Physico-chemical Properties
| Molecular Formula | C12H11NO3 |
| Molar Mass | 217.22 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD03768192 |
2-(aminomethyl)-5-phenyl-3-furoic acid hydrochloride - Introduction
Acid is an organic compound with the chemical formula C13H12N2O3.
Some of its properties are as follows:
-Appearance: White crystalline solid
-Melting point: about 180-182°C
-Solubility: Slightly soluble in water, soluble in organic solvents such as ethanol and dimethylformamide
It can be used to synthesize various organic compounds and drugs. It acts as a precursor to chimeras or ligands and can be used in coordination chemistry and drug design. It can also be used as a biological fluorescent probe and an analytical reagent.
The method of preparing phosphonic acid generally involves the following steps: First, 2-nitro-5-phenyl-furan-3-carbaldehyde is synthesized through a nitrosylation reaction. The compound was then reduced with sodium sulfite to give 2-aminomethyl-5-phenyl-furan-3-carbaldehyde. Finally, the aldehyde compound obtained is converted into the target product N-acid by an amination reaction.
Regarding safety information, since it is an organic compound, care should be taken to prevent inhalation, contact with skin and eyes. It should be used in a well-ventilated area with appropriate personal protective measures, such as gloves and masks. If accidental contact or inhalation, should immediately rinse with water, and timely medical treatment.
Some of its properties are as follows:
-Appearance: White crystalline solid
-Melting point: about 180-182°C
-Solubility: Slightly soluble in water, soluble in organic solvents such as ethanol and dimethylformamide
It can be used to synthesize various organic compounds and drugs. It acts as a precursor to chimeras or ligands and can be used in coordination chemistry and drug design. It can also be used as a biological fluorescent probe and an analytical reagent.
The method of preparing phosphonic acid generally involves the following steps: First, 2-nitro-5-phenyl-furan-3-carbaldehyde is synthesized through a nitrosylation reaction. The compound was then reduced with sodium sulfite to give 2-aminomethyl-5-phenyl-furan-3-carbaldehyde. Finally, the aldehyde compound obtained is converted into the target product N-acid by an amination reaction.
Regarding safety information, since it is an organic compound, care should be taken to prevent inhalation, contact with skin and eyes. It should be used in a well-ventilated area with appropriate personal protective measures, such as gloves and masks. If accidental contact or inhalation, should immediately rinse with water, and timely medical treatment.
Last Update：2024-04-09 21:04:16
