TIMTEC-BB SBB010834

TIMTEC-BB SBB010834 - Names and Identifiers

Name	(2-aminophenyl)(pyrrolidin-1-yl)methanone
Synonyms	TIMTEC-BB SBB010834 1-(2-Aminobenzoyl)pyrrolidine 2-(1-pyrrolidinylcarbonyl)aniline 2-(PYRROLIDIN-1-YLCARBONYL)ANILINE [2-(PYRROLIDIN-1-YLCARBONYL)PHENYL]AMINE (2-aminophenyl)(pyrrolidin-1-yl)methanone (2-Amino-phenyl)-pyrrolidin-1-yl-methanone (2-AMINO-PHENYL)-PYRROLIDIN-1-YL-METHANONE methanone, (2-aminophenyl)-1-pyrrolidinyl- [2-(pyrrolidin-1-ylcarbonyl)phenyl]amine hydrochloride
CAS	52745-20-7
InChI	InChI=1/C11H14N2O/c12-10-6-2-1-5-9(10)11(14)13-7-3-4-8-13/h1-2,5-6H,3-4,7-8,12H2

TIMTEC-BB SBB010834 - Physico-chemical Properties

Molecular Formula	C11H14N2O
Molar Mass	190.24
Density	1.195g/cm³
Boling Point	376.1°C at 760 mmHg
Flash Point	181.2°C
Vapor Presure	7.44E-06mmHg at 25°C
Storage Condition	Room Temprature
Refractive Index	1.62

TIMTEC-BB SBB010834 - Risk and Safety

Hazard Symbols	Xi - Irritant
Hazard Class	IRRITANT

TIMTEC-BB SBB010834 - Introduction

(2-aminophenyl)(pyrrolidin-1-yl)methanone is an organic compound whose molecular formula is C12H14N2O. The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
(2-aminophenyl)(pyrrolidin-1-yl)methanone is a solid with white or off-white crystal morphology. It is a compound that is soluble in organic solvents (such as ethanol, dimethylformamide), but has a low solubility in water. This compound is stable at room temperature, but may decompose under high temperature conditions.

Use:
(2-aminophenyl)(pyrrolidin-1-yl)methanone has a wide range of applications in organic synthesis. It can be used as an intermediate for the synthesis of various organic compounds with biological activity. For example, it can be used to synthesize compounds such as drugs, dyes and pesticides. In addition, the compound can also be used in the preparation of organic photoelectric materials and other fields.

Preparation Method:
(2-aminophenyl)(pyrrolidin-1-yl)methanone can be prepared by the following method: first, reacting 2-aminobenzoic acid with pyrrolidine aldehyde to obtain (2-aminophenyl)(pyrrolidin-l-yl) carboxylic acid; then, reacting the obtained acid with ammonia carbonate, and removing the protecting group to obtain (2-aminophenyl)(pyrrolidin-1-yl)methanone.

Safety Information:
(2-aminophenyl)(pyrrolidin-1-yl)methanone safety information is limited. Due to its chemical nature, it should be used in accordance with routine chemical laboratory safety procedures. The compound may be irritating to the skin, eyes and respiratory system. Direct contact with skin and eyes should be avoided and good ventilation should be maintained. During operation and storage, the production of flammable gases and vapors should be avoided.

Last Update：2024-04-09 21:04:16