(3-Oxopiperazin-2-yl)acetic acid
(3-Oxopiperazin-2-yl)acetic acid
CAS: 405214-33-7
Molecular Formula: C6H10N2O3
(3-Oxopiperazin-2-yl)acetic acid - Names and Identifiers
(3-Oxopiperazin-2-yl)acetic acid - Physico-chemical Properties
| Molecular Formula | C6H10N2O3 |
| Molar Mass | 158.16 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD04226363 |
(3-Oxopiperazin-2-yl)acetic acid - Introduction
(3-Oxopiperazin-2-yl)acetic acid, also known as (3-Oxopiperazin-2-yl)acetic acid, has the following chemical structure:
CH3CH2C(O)NHCH2(C=O)N1CC(O)C(C1)=O
The properties of the compound are as follows:
-Appearance: Colorless solid
-Molecular formula: C8H11N3O4
-Molecular weight: 221.19g/mol
-Melting point: 134-136 degrees Celsius
-Solubility: Soluble in water and common organic solvents
The main applications of (3-Oxopiperazin-2-yl)acetic acid include:
-Pharmaceutical research: as an intermediate or starting material for the synthesis of drugs, peptides and biologically active molecules.
-Drug delivery system: It can be used to prepare a sustained-release agent to help control the release rate of the drug.
-Membrane material: The polymer of this compound can be used in the fields of membrane separation and membrane filtration.
(3-Oxopiperazin-2-yl)acetic acid has two common methods:
1. reaction of piperazine and bromoacetic acid: first, piperazine reacts with sodium hydroxide to generate the corresponding salt. The piperazine salt is then reacted with bromoacetic acid to give (3-Oxopiperazin-2-yl)acetic acid.
2. reaction of acetic acid chloride and (3-oxopiperazin -2-yl) ethanol: acetic acid chloride and (3-oxopiperazin -2-yl) ethanol are reacted under the catalysis of base to generate (3-Oxopiperazin-2-yl)acetic acid.
Security information about (3-Oxopiperazin-2-yl)acetic acid:
-The compound is an organic compound with certain toxicity and irritation, so it needs to be used and handled under suitable experimental conditions.
-Avoid direct contact with skin, eyes and respiratory tract during use and handling, and wear appropriate protective measures such as gloves, glasses and respirators when necessary.
-In the event of accidental exposure or inhalation overdose, clean the area immediately and seek medical attention.
-During storage and transportation, it should be kept in a cool and dry place to avoid contact with oxidants, strong acids and strong bases.
CH3CH2C(O)NHCH2(C=O)N1CC(O)C(C1)=O
The properties of the compound are as follows:
-Appearance: Colorless solid
-Molecular formula: C8H11N3O4
-Molecular weight: 221.19g/mol
-Melting point: 134-136 degrees Celsius
-Solubility: Soluble in water and common organic solvents
The main applications of (3-Oxopiperazin-2-yl)acetic acid include:
-Pharmaceutical research: as an intermediate or starting material for the synthesis of drugs, peptides and biologically active molecules.
-Drug delivery system: It can be used to prepare a sustained-release agent to help control the release rate of the drug.
-Membrane material: The polymer of this compound can be used in the fields of membrane separation and membrane filtration.
(3-Oxopiperazin-2-yl)acetic acid has two common methods:
1. reaction of piperazine and bromoacetic acid: first, piperazine reacts with sodium hydroxide to generate the corresponding salt. The piperazine salt is then reacted with bromoacetic acid to give (3-Oxopiperazin-2-yl)acetic acid.
2. reaction of acetic acid chloride and (3-oxopiperazin -2-yl) ethanol: acetic acid chloride and (3-oxopiperazin -2-yl) ethanol are reacted under the catalysis of base to generate (3-Oxopiperazin-2-yl)acetic acid.
Security information about (3-Oxopiperazin-2-yl)acetic acid:
-The compound is an organic compound with certain toxicity and irritation, so it needs to be used and handled under suitable experimental conditions.
-Avoid direct contact with skin, eyes and respiratory tract during use and handling, and wear appropriate protective measures such as gloves, glasses and respirators when necessary.
-In the event of accidental exposure or inhalation overdose, clean the area immediately and seek medical attention.
-During storage and transportation, it should be kept in a cool and dry place to avoid contact with oxidants, strong acids and strong bases.
Last Update：2024-04-09 21:54:55
