N-BOC-3,3-AMINO-PIPERIDINYLCARBOXYLIC ACID - Names and Identifiers
N-BOC-3,3-AMINO-PIPERIDINYLCARBOXYLIC ACID - Physico-chemical Properties
Molecular Formula | C11H20N2O4
|
Molar Mass | 244.29 |
Density | 1.203±0.06 g/cm3(Predicted) |
Boling Point | 380.1±42.0 °C(Predicted) |
Flash Point | 192.53°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 2.26±0.20(Predicted) |
Storage Condition | 2-8°C(protect from light) |
Refractive Index | 1.595 |
N-BOC-3,3-AMINO-PIPERIDINYLCARBOXYLIC ACID - Introduction
Acid (also known as Boc-APP acid) is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: A white crystalline solid.
-Molecular formula: C13H22N2O4
-Molecular weight: 270.33g/mol
-Melting point: about 128 degrees Celsius
-Solubility: Soluble in chloroform, dichloromethane and dimethyl sulfoxide, insoluble in water.
Use:
-the acid is often used as a starting material and intermediate in organic synthesis.
-It can be used to synthesize drugs, pesticides and other biologically active compounds.
Preparation Method:
-tert-acid can be synthesized by the following methods: First, 1-piperidinecarboxylic acid and tert-butyl dichloroformamide (Boc-Cl) are reacted to obtain 1-Boc-3-tert-butyl piperidine. 1-Boc-3-tert-butylpiperidine is then reacted with bromoacetic acid to produce 1-Boc-3-aminopiperidine-3-acetic acid. Finally, acid is obtained by hydrolytic esterification.
Safety Information:
-the acid is relatively safe under normal operation.
-Avoid contact with strong oxidants during use.
-Wear gloves and laboratory coats during operation, and ensure good ventilation.
-In case of accidental use or contact with skin or eyes, rinse with plenty of water and seek medical help.
Last Update:2024-04-09 21:01:54