1190129-81-7

Basic information

• Product Name: 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile
• Synonyms: 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile
• CAS NO: 1190129-81-7
• Molecular Formula: C₁₇H₁₆N₂O
• Molecular Weight: 264.32174
• Mol File: 1190129-81-7.mol
• Article Data: 34

Chemical Properties

• Boiling Point: 486.7±45.0 °C(Predicted)
• Appearance: /
• Density: 1.20±0.1 g/cm3(Predicted)
• PKA: 2.08±0.60(Predicted)
• CAS DataBase Reference: 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile(1190129-81-7)
• EPA Substance Registry System: 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile(1190129-81-7)

Safety Data

• Hazardous Substances Data: 1190129-81-7(Hazardous Substances Data)

Usage

General Description

1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile is a chemical compound with the molecular formula C18H18N2O. It is a member of the isoquinoline class of compounds and contains a nitrile functional group. This chemical is a white solid at room temperature and is insoluble in water. It is commonly used as a research reagent in the field of organic chemistry and pharmaceutical development. The compound has been studied for its potential biological activities and is of interest due to its structural similarities to other biologically active molecules. It has also been investigated for its potential applications in medicinal chemistry. Overall, 1,2,3,4-tetrahydro-2-(4-Methoxyphenyl)-1-Isoquinolinecarbonitrile is a versatile chemical that has potential uses in various scientific and industrial applications.

Upstream product

• 78317-83-6 2-(4-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline 
• 7677-24-9 trimethylsilyl cyanide 
• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 109-77-3 malononitrile 
• 102-96-5 (2-nitroethenyl)benzene 
• 100-52-7 benzaldehyde 
• 64-04-0 phenethylamine 
• 773837-37-9 sodium cyanide 
• 110-71-4 1,2-dimethoxyethane 
• 75-05-8 acetonitrile 
• 68-12-2 N,N-dimethyl-formamide 
• 107-06-2 1,2-dichloro-ethane 
• 109-99-9 tetrahydrofuran 
• 108-88-3 toluene 

Downstream Products

• 1132765-82-2 1-(aminomethyl)-2-(4-methoxyphenyl)-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Electrochemically promoted oxidative α-cyanation of tertiary and secondary amines using cheap AIBN

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Donor-acceptor type [4+3] covalent organic frameworks: sub-stoichiometric synthesis and photocatalytic application

Three unprecedented 2D [4+3] covalent organic frameworks (TTCOF-1, TTCOF-2, and TTCOF-3) have been prepared by substoichiometric condensation of tetratopic and tritopic monomers, overcoming the limitations of the design rules of conventional topologies. By reticulating the tetraphenylethylene (TPE)-based and triazine-based moieties into COF frameworks, novel electron donor-acceptor (D-A) type structures were obtained. These TTCOFs have good photocatalytic activity in aerobic C(sp3)-H bond functionalization and arylboronic acid oxidation driven by visible light, with yields up to 94%. This can expedite possibilities of COFs with new structural and topological complexities and can also expand the application of COF-based photocatalysis in synthetic chemistry.