247132-40-7

Basic information

• Product Name: 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester
• CAS NO: 247132-40-7
• Molecular Formula: C17H17NO3
• Molecular Weight: 283.327
• Mol File: 247132-40-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester(247132-40-7)
• EPA Substance Registry System: 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester(247132-40-7)

Safety Data

• Hazardous Substances Data: 247132-40-7(Hazardous Substances Data)

Usage

General Description

2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester is a chemical compound that belongs to the class of isoquinolinecarboxylic acids. It is a derivative of isoquinolinecarboxylic acid, with an added phenylmethyl ester group. 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester has been identified as having potential pharmacological activities, including antimicrobial and anticancer properties. It has been studied for its potential use in the development of new drug treatments, particularly for bacterial and cancer diseases. 2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-7-hydroxy-, phenylmethyl ester is of interest to researchers and pharmaceutical companies as a potential lead molecule for drug development.

Upstream product

• 110192-19-3 7-hydroxy-1,2,3,4-tetrahydroisoquinoline hydrobromide 
• 501-53-1 benzyl chloroformate 
• 39989-39-4 7-methoxyisoquinoline 
• 43207-78-9 7-methoxy-1,2,3,4-tetrahydroisoquinoline 
• 7651-83-4 isoquinolin-7-ol 

Downstream Products

• 247132-41-8 benzyl 7-methylthiomethoxy-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247133-11-5 7-[2-(1-tert-butoxycarbonyl-4-cyanopiperidin-4-yl)ethoxy]-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid benzyl ester 
• 1206698-01-2 7-(4-ethoxycarbonyl-phenoxy)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester 
• 247132-52-1 benzyl 7-(2-iodoethoxy)-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 832088-74-1 benzyl 7-[4-ethoxycarbonyl-1-(pyridin-4-yl)piperidin-4-ylmethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-42-9 7-chloromethoxy-3,4-dihydro-1H-isoquinolin-2-carboxylate benzyl ester 
• 854261-77-1 benzyl 7-[1-(1-amidinophenyl-4-yl)-4-ethoxycarbonylpiperidin-4-ylmethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-53-2 benzyl 7-[2-(1-tert-butoxycarbonyl-4-ethoxycarbonylpiperidin-4-yl)ethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-49-6 benzyl 7-[4-ethoxycarbonyl-1-(2-methylpyridin-4-yl)piperidin-4-ylmethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-50-9 benzyl 7-[1-(2-chloropyrimidin-4-yl)-4-ethoxycarbonylpiperidin-4-ylmethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-54-3 benzyl 7-[2-[4-ethoxycarbonyl-1-(pyridin-4-yl)piperidin-4-yl]ethoxy]-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-46-3 benzyl 7-(1-tert-butoxycarbonyl-4-ethoxycarbonylpiperidin-4-ylmethoxy)-1,2,3,4-tetrahydroisoquinolin-2-carboxylate 
• 247132-47-4 7-(4-ethoxycarbonylpiperidin-4-ylmethoxy)-1,2,3,4-tetrahydroisoquinoline-2-carboxylic acid benzyl ester 

Relevant articles and documents

Synthesis and structure-activity relationships of novel selective factor Xa inhibitors with a tetrahydroisoquinoline ring

A series of novel 2,7-disubstituted tetrahydroisoquinoline derivatives were designed and synthesized. Among these derivatives, compounds 1 and 2 exhibited potent inhibitory activity against factor Xa (FXa) and good selectivity with respect to other serine

Amidine compounds

A compound of the formula [I] wherein R1, R2and R3are the same or different and each is hydrogen atom, wherein each symbol is as defined in the specification, a salt thereof or a prodrug thereof. The compound of the presen