4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID

4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID - Names and Identifiers

Name	(S)-1-Boc-piperazine-3-carboxylic acid
Synonyms	(S)-1-Boc-piperazine-3-carboxylic acid 4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID (S)-4-Boc-piperazine-2-carboxylic acid S-4-N-BOC-2-PIPERIDINE CARBOXYLIC ACID S-4-N-BOC-2-CARBOXYLIC ACID PIPERAZINE (S)-1-N-Boc-piperazine-3-carboxylic acid (S)-4-N-Boc-Piperazine-2-carboxylic acid (S)-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID (S)-4-(TERT-BUTOXYCARBONYL)PIPERAZINE-2-CARBOXYLIC ACID (S)-PIPERAZINE-1,3-DICARBOXYLIC ACID 1-TERT-BUTYL ESTER
CAS	848482-93-9

4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID - Physico-chemical Properties

Molecular Formula	C10H18N2O4
Molar Mass	230.26
Density	1.193±0.06 g/cm3(Predicted)
Melting Point	231-239 ºC
Boling Point	371.8±37.0 °C(Predicted)
Appearance	Crystalline powder
pKa	2.20±0.20(Predicted)
Storage Condition	2-8°C(protect from light)

4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	R36 - Irritating to the eyes R43 - May cause sensitization by skin contact
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37 - Wear suitable protective clothing and gloves.

4-BOC-PIPERAZINE-2-(S)-CARBOXYLIC ACID - Introduction

(S)-I acid is an organic compound with the chemical name (S)-I acid. It is a colorless crystal, stable at room temperature. The following is a description of its nature, use, formulation and safety information:

Nature:
(S)-acid has a molecular formula of C11H18N2O4 and a molecular weight of 246.27g/mol. It has two stereoisomers, of which (S)-phosphonic acid is one of them. It has a melting point of 110-111°C and is a highly soluble compound that is soluble in a variety of common organic solvents.

Use:
(S)-acid is widely used in organic synthesis. It can be used as a chiral skeleton and chiral inducer for the synthesis of other chiral compounds. It can be used as an intermediate in the synthesis of drugs, the synthesis of chiral ligands, etc. In addition, it can also be used for the synthesis of piperazine compounds and other organic compounds.

Preparation Method:
The preparation of (S)-acid usually starts by synthesizing piperazine compounds, and carboxyl protection and protonation reactions are carried out on piperazine compounds to obtain the target product. The specific preparation method is complicated and requires the use of suitable reaction reagents and conditions.

Safety Information:
(S)-acid is relatively safe under normal conditions of use, but you still need to pay attention to the following:
-Avoid direct contact with the skin and inhalation of its dust or solution during operation.
-Wear appropriate personal protective equipment, such as lab gloves and goggles.
-Store it in a dry, cool place and away from fire and oxidizing agents.
-Observe relevant safety operations and specifications during use and handling.
-In the event of misuse or direct contact, seek medical attention immediately and bring the product packaging to the hospital.

Last Update：2024-04-09 20:52:54