23019-62-7

Basic information

• Product Name: Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate
• Synonyms: 1-Benzyl-1,2,3,6-tetrahydroisonicotinic acid ethyl ester;Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate;Ethyl 1-benzyl-1,2,3,6-tetrahydroisonicotinate
• CAS NO: 23019-62-7
• Molecular Formula: C₁₅H₁₉NO₂
• Molecular Weight: 245.32
• Product Categories: API intermediates
• Mol File: 23019-62-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 344 °C
• Flash Point: 121 °C
• Appearance: /
• Density: 1.108
• Vapor Pressure: 6.78E-05mmHg at 25°C
• Refractive Index: 1.554
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate(23019-62-7)
• EPA Substance Registry System: Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate(23019-62-7)

Safety Data

• Hazardous Substances Data: 23019-62-7(Hazardous Substances Data)

Usage

General Description

Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate is a chemical compound with the molecular formula C17H21NO2. It is commonly used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. This chemical is a tetrahydropyridine derivative, which is a class of compounds known for their diverse pharmacological activities. Ethyl 1-benzyl-1,2,3,6-tetrahydropyridine-4-carboxylate has potential applications in the development of new drugs for the treatment of various medical conditions. It is important to handle and use this chemical with care, following all necessary safety precautions and regulations.

InChI:InChI=1/C15H19NO2/c1-2-18-15(17)14-8-10-16(11-9-14)12-13-6-4-3-5-7-13/h3-8H,2,9-12H2,1H3

Upstream product

• 1570-45-2 isonicotinic acid ethylester 
• 100-39-0 benzyl bromide 
• 23019-61-6 1-benzyl-4-(ethoxycarbonyl)pyridin-1-ium bromide 

Relevant articles and documents

Metal-free reduction of unsaturated carbonyls, quinones, and pyridinium salts with tetrahydroxydiboron/water

A series of unsaturated carbonyls, quinones, and pyridinium salts have been effectively reduced to the corresponding saturated carbonyls, dihydroxybenzenes, and hydropyridines in moderate to high yields with tetrahydroxydiboron/water as a mild, convenient, and metal-free reduction system. Deuterium-labeling experiments have revealed this protocol to be an exclusive transfer hydrogenation process from water. This journal is

New anti-MRSA and anti-VRE carbapenems: Synthesis and structure-activity relationships of 1β-metyl-2-(thiazol-2-ylthio)carbapenems

Discovery of novel antimicrobial agents effective against infections caused by drug-resistant pathogens is an important objective. In order to find a new parenteral carbapenem antibiotic, which has potent antibacterial activity especially against methicillin-resistant staphylococci, vancomycin-resistant enterococci and penicillin-resistant Streptococcus pneumoniae, a series of 1β-methylcarbapenems with thiazol-2-ylthio groups at the C-2 position have been synthesized. Structure-activity relationships were investigated which led to SM-197436 (27), SM-232721 (44) and SM-232724 (41), being selected for further evaluation.