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4-Methoxyisoquinoline is a chemical compound that belongs to the class of isoquinoline alkaloids. It is a derivative of isoquinoline, characterized by the presence of a methoxy group on the 4th carbon atom of the isoquinoline ring. 4-Methoxyisoquinoline has demonstrated a range of biological activities, such as antioxidant and antimicrobial properties, and is being explored for its potential in the pharmaceutical industry, particularly for its ability to inhibit the growth of certain cancer cells. Furthermore, it has shown promise as a fluorescent probe in the fields of analytical chemistry and bioimaging.

36034-54-5

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36034-54-5 Usage

Uses

Used in Pharmaceutical Industry:
4-Methoxyisoquinoline is used as a potential drug candidate for its ability to inhibit the growth of certain cancer cells, making it a valuable asset in the development of new anticancer therapies.
Used in Analytical Chemistry:
4-Methoxyisoquinoline is used as a fluorescent probe due to its optical properties, which allow for its application in various analytical techniques and detection methods.
Used in Bioimaging Applications:
4-Methoxyisoquinoline is utilized as a fluorescent marker in bioimaging, enabling the visualization and tracking of biological processes at the molecular level, which is crucial for understanding disease mechanisms and developing targeted therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 36034-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,3 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36034-54:
(7*3)+(6*6)+(5*0)+(4*3)+(3*4)+(2*5)+(1*4)=95
95 % 10 = 5
So 36034-54-5 is a valid CAS Registry Number.

36034-54-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Methoxyisoquinoline

1.2 Other means of identification

Product number -
Other names 4-Methoxy-isoquinoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36034-54-5 SDS

36034-54-5Downstream Products

36034-54-5Relevant academic research and scientific papers

Oxidative Addition Complexes as Precatalysts for Cross-Coupling Reactions Requiring Extremely Bulky Biarylphosphine Ligands

Ingoglia, Bryan T.,Buchwald, Stephen L.

supporting information, p. 2853 - 2856 (2017/06/07)

In this report, we describe the application of palladium-based oxidative addition complexes (OACs) as effective precatalysts for C-N, C-O, and C-F cross-coupling reactions with a variety of (hetero)arenes. These complexes offer a convenient alternative to previously developed classes of precatalysts, particularly in the case of the bulkiest biarylphosphine ligands, for which palladacycle-based precatalysts do not readily form. The precatalysts described herein are easily prepared and stable to long-term storage under air.

Mild and general palladium-catalyzed synthesis of methyl aryl ethers enabled by the use of a palladacycle precatalyst

Cheung, Chi Wai,Buchwald, Stephen L.

supporting information, p. 3998 - 4001 (2013/09/02)

A general method for the Pd-catalyzed coupling of methanol with (hetero)aryl halides is described. The reactions proceed under mild conditions with a wide range of aryl and heteroaryl halides to give methyl aryl ethers in high yield.

HEPATITIS C VIRUS INHIBITORS

-

Page 305, (2008/06/13)

Hepatitis C virus inhibitors are disclosed having the general formula:(I) wherein R1, R2, R3, R', B, Y and X are described in the description. Compositions comprising the compounds and methods for using the compounds toinhibit HCV are also disclosed.

Photochemistry of Methoxy-substituted Quinoline and Isoquinoline N-Oxides

Albini, Angelo,Fasani, Elisa,Dacrema, Lucia Maggi

, p. 2738 - 2742 (2007/10/02)

The photochemistry of quinoline 1-oxides and isoquinoline 2-oxides bearing a methoxy-group in the pyridine ring was investigated in protic and aprotic media.The formation of various photoisomers, viz. 3,1-benzoxazepines, 2(1H)-quinolones, N-(2-isocyanobenzyl)formamides, 4(1H)-quinolones, and 3-hydroxyquinolines from the different methoxyquinoline 1-oxides, and 1,3-benzoxazepines and 1(2H)-isoquinolones from the different methoxyisoquinoline 2-oxides, was observed along with deoxygenation and formation of products derived from hydration and decomposition of the primary products.The position of the methoxy-group has an important directing effect on the photoreactions.

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