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58021-73-1

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58021-73-1 Usage

Derivative of isoquinoline

The compound is derived from the isoquinoline structure, which is a tricyclic aromatic system consisting of two benzene rings fused to a six-membered nitrogen-containing ring.

Presence of benzoyl and methoxy groups

The compound contains a benzoyl group (a carbonyl group attached to a benzene ring) and a methoxy group (an oxygen atom attached to a methyl group), which are responsible for its structural features and potential biological activity.

Potential applications in pharmaceutical research and drug development

Due to its unique structure, the compound may have biological activity that could be useful in the development of new drugs and therapies.

Need for further studies

To determine the specific properties and potential uses of 2-(4-methoxybenzoyl)-1,2-dihydroisoquinoline-1-carbonitrile in medicine, additional research and analysis are required. This may include testing for pharmacological activity, toxicity, and other relevant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 58021-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,2 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 58021-73:
(7*5)+(6*8)+(5*0)+(4*2)+(3*1)+(2*7)+(1*3)=111
111 % 10 = 1
So 58021-73-1 is a valid CAS Registry Number.

58021-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxybenzoyl)-1H-isoquinoline-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 1,2-dihydro-2-(4-methoxybenzoyl)isoquinoline-1-carbonitrile

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:58021-73-1 SDS

58021-73-1Relevant articles and documents

Protoberberines from Reissert-Compounds VIII [1]. Oxazoloisoquinolines, New and Efficient Educts for the Synthesis of 8-Oxoprotoberberines

Reimann, Eberhard,Grasberger, Fritz,Polborn, Kurt

, p. 991 - 1014 (2007/10/03)

Certain benzylated oxazoloisoquinolinones readily available from Reissert compounds provided an efficient access to 8-oxoprotoberberines in three steps. A series of these new precursors as well as several oxoprotoberberines were prepared and the scope and limitation of this procedure were investigated.

REISSERT COMPOUND STUDIES LXIII: PREPARATION OF REISSERT COMPOUNDS USING DIETHYLALUMINIUM CYANIDE

Duarte, Frederick F.,Popp, Frank D.

, p. 723 - 726 (2007/10/02)

Reissert compounds and analogs were synthesized from the reaction of acid halide, heterocyclic base and diethylaluminium cyanide.This new method of Reissert compound synthesis gave yields comparable to other synthetic routes.

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