58028-74-3

Basic information

• Product Name: 2-PYRROLIDIN-1-YLBENZALDEHYDE
• Synonyms: 2-PYRROLIDIN-1-YLBENZALDEHYDE;ASINEX-REAG BAS 10156458;TIMTEC-BB SBB010579;2-Pyrrolidin-1-ylbenzaldehyde 97%;2-(1-Pyrrolidinyl)benzaldehyde;2-Pyrrolidinobenzaldehyde;2-(Pyrrolidin-1-yl)benzaldehyde97%
• CAS NO: 58028-74-3
• Molecular Formula: C₁₁H₁₃NO
• Molecular Weight: 175.23
• Product Categories: Carbonyl Compounds;Heterocycles
• Mol File: 58028-74-3.mol
• Article Data: 32

Chemical Properties

• Boiling Point: 307.4 °C at 760 mmHg
• Flash Point: 120.7 °C
• Appearance: /
• Density: 1.125 g/cm³
• Vapor Pressure: 0.000516mmHg at 25°C
• Refractive Index: 1.573
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-PYRROLIDIN-1-YLBENZALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PYRROLIDIN-1-YLBENZALDEHYDE(58028-74-3)
• EPA Substance Registry System: 2-PYRROLIDIN-1-YLBENZALDEHYDE(58028-74-3)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 58028-74-3(Hazardous Substances Data)

Usage

General Description

2-Pyrrolidin-1-ylbenzaldehyde is an organic compound with the chemical formula C12H13NO. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is a yellowish liquid with a sweet, floral odor, and it is soluble in organic solvents. It is known to have potential applications in the fragrance industry as a raw material for the production of perfumes and flavorings. Additionally, 2-Pyrrolidin-1-ylbenzaldehyde may also have potential applications in the field of organic synthesis, particularly in the development of new chemical compounds for various industrial and research purposes.

InChI:InChI=1/C11H9NO/c13-9-10-5-1-2-6-11(10)12-7-3-4-8-12/h1-9H

Upstream product

• 123-75-1 pyrrolidine 
• 446-52-6 2-Fluorobenzaldehyde 
• 89-98-5 2-chloro-benzaldehyde 
• 73051-88-4 [2-(pyrrolidin-1-yl)phenyl]methanol 

Downstream Products

• 83716-79-4 2-Pyrrolidinocinnamic acid 
• 135064-80-1 (E)-2-Cyano-3-(2-pyrrolidin-1-yl-phenyl)-acrylic acid butyl ester 
• 73051-88-4 [2-(pyrrolidin-1-yl)phenyl]methanol 
• 218934-27-1 1-(2-Formylphenyl)-2-pyrrolidon 
• 1092982-59-6 4-(2-(1H-indol-3-yl)ethyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-60-9 1-(2-(pyrrolidin-1-yl)phenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 
• 1092982-42-7 4-(2-fluorolphenyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-38-1 4-(2,6-diisopropylphenyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-39-2 4-(4-methoxylphenyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-36-9 4-phenyl-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-56-3 4-(1-phenylethyl)-1,2,3,4a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 22462-30-2 4-benzyl-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-41-6 4-(4-bromolphenyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 
• 1092982-37-0 4-(4-ethylphenyl)-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinazoline 

Relevant articles and documents

HPLC-ECD and TDDFT-ECD study of hexahydropyrrolo[1,2-a]quinoline derivatives

Synthesis of racemic hexahydropyrrolo[1,2-a]quinoline derivatives (1-8) was performed by utilizing the Knoevenagel-[1,5]-hydride shift-cyclization domino reaction. Separation of the enantiomers of the chiral products (1-8) was carried out by chiral high-p

Double Capture of Difluorocarbene by 2-Aminostyrenes Enables the Construction of 3-(2,2-Difluoroethyl)-2-fluoroindoles

We report herein an efficient strategy to construct 3-(2,2-difluoroethyl)-2-fluoroindoles from activated o-aminostyrenes with ethyl bromodi-fluoroacetate as a difluorocarbene source. Through double capture of a difluorocarbene, two different types of fluo

Development of TsDPEN based imine-containing ligands for the copper-catalysed asymmetric Kinugasa reaction

A novel class of chiralN,N,Nimine-containing ligands derived from TsDPEN (N-(p-tosyl)-1,2-diphenylethylene-1,2-diamine) has been developed and applied to the copper-catalyzed asymmetric Kinugasa reaction. The copper(ii) salt proved to be an efficient catalyst precursor, and it provides an efficient way to synthesize enantioenrichedcis-β-lactam. The pathway is air-tolerant and easily manipulated, and the ligands are easy to synthesize. A working model is proposed in which the stereocontrolling step is the [2 + 2] cycloaddition between ketene and imine to explain the observed stereoselectivities.

4-(2-(pyrrolidine/piperidine-1-yl)benzyl)-piperazine urea TRPV1 antagonist and preparation method and application thereof

The invention discloses a novel 4-(2-(pyrrolidine/piperidine-1-yl)benzyl)-piperazine urea type TRPV1 antagonist and a preparation method and application thereof. The invention relates to a compound ina general formula (I) and a pharmaceutically acceptable