2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE

2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE - Names and Identifiers

Name	2-pyrrolidin-1-ylpyridine-4-carboxylic acid
Synonyms	2-pyrrolidinoisonicotinic acid 2-(Pyrrolidin-1-yl)isonicotinic acid 2-pyrrolidin-1-ylpyridine-4-carboxylic acid 2-(1-Pyrrolidinyl)-4-pyridinecarboxylic acid 4-Pyridinecarboxylic acid, 2-(1-pyrrolidinyl) (2-Pyrrolidin-1-yl)pyridine-4-carboxylic acid 4-pyridinecarboxylic acid, 2-(1-pyrrolidinyl)- 2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE 2-pyrrolidin-1-ylpyridine-4-carboxylic acid hydrate 4-Pyridinecarboxylic acid, 2-(1-pyrrolidinyl)(HCl salt)
CAS	98088-04-1
InChI	InChI=1/C10H12N2O2.H2O/c13-10(14)8-3-4-11-9(7-8)12-5-1-2-6-12;/h3-4,7H,1-2,5-6H2,(H,13,14);1H2

2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE - Physico-chemical Properties

Molecular Formula	C10H12N2O2
Molar Mass	192.21
Melting Point	211 °C
Boling Point	556.8°C at 760 mmHg
Flash Point	290.6°C
Vapor Presure	3.1E-13mmHg at 25°C
Storage Condition	2-8°C

2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE - Risk and Safety

Hazard Note

Irritant

2-PYRROLIDIN-1-YL-ISONICOTINIC ACID HYDROCHLORIDE - Introduction

Acid is an organic compound with the chemical formula C11H13NO2. The following is a description of its nature, use, preparation and safety information:

Nature:
-acrylic is a solid, available as an anhydrous form, colorless or light yellow crystals.
-It is soluble in some organic solvents such as methanol, ethanol and dimethylformamide at room temperature, but insoluble in water.
-In terms of chemical properties, it can be catalyzed by acid or base addition reaction, and the condensation reaction of carboxylic acid and amine group occurs.

Use:
-must acid is often used as an intermediate or catalyst in organic synthesis.
-It can be used to synthesize pyrrolidine compounds, such as oxalyl ester pesticides.
-In addition, it can also be used to prepare biologically active compounds, such as drug molecules.

Preparation Method: There are many synthesis methods of
-pyridyl acid. A common preparation method is to generate 2-pyrrolidinyl-pyridine through the reaction of pyridine and pyrrolidine aldehyde, and then introduce carboxylic acid groups through carboxylation reaction to obtain the target product.

Safety Information:
-the use of acid under normal laboratory conditions generally does not pose much safety risk.
-However, as a chemical, it still needs to be handled and stored properly.
-Use in accordance with safety procedures, wear personal protective equipment such as gloves and glasses, and avoid contact with skin and eyes.
-When disposing of waste, it should be disposed of in accordance with local regulations.

Please note that the above information is for reference only. If you need to use this compound or perform related experiments, please follow the relevant safety operating instructions under laboratory conditions and comply with local regulations.

Last Update：2024-04-09 20:45:29