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5-Bromo-8-chloroisoquinoline, with the molecular formula C9H5BrClN, is a yellow crystalline solid that serves as a versatile building block in the synthesis of pharmaceuticals and agrochemicals. Its chemical structure allows for participation in various organic reactions, such as Suzuki coupling and palladium-catalyzed cross-coupling reactions, making it a valuable compound in the development of new materials and as a reagent in chemical research.

956003-79-5

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956003-79-5 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
5-Bromo-8-chloroisoquinoline is used as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its chemical properties enable it to be a key component in the creation of novel therapeutic agents and crop protection products.
Used in Organic Reactions:
5-BROMO-8-CHLOROISOQUINOLINE is utilized as a reactant in various organic reactions, including Suzuki coupling and palladium-catalyzed cross-coupling reactions. Its participation in these reactions facilitates the formation of new chemical entities with potential applications in different fields.
Used in the Preparation of Fluorescent Probes and Dyes:
5-Bromo-8-chloroisoquinoline is employed in the preparation of fluorescent probes and dyes for biological imaging. Its fluorescent properties make it suitable for use in the development of imaging agents that can be used to visualize biological processes and structures.
Used in the Development of New Materials:
5-BROMO-8-CHLOROISOQUINOLINE has potential applications in the development of new materials, where its unique chemical properties can be harnessed to create innovative products with specific characteristics.
Used as a Reagent in Chemical Research:
5-Bromo-8-chloroisoquinoline serves as a reagent in chemical research, where it is used to study various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge in the field of chemistry.
It is important to handle 5-bromo-8-chloroisoquinoline with care, as it may be harmful if ingested or inhaled and can cause irritation upon contact with skin and eyes. Proper safety measures should be taken during its use to ensure the well-being of individuals working with 5-BROMO-8-CHLOROISOQUINOLINE.

Check Digit Verification of cas no

The CAS Registry Mumber 956003-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,0,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 956003-79:
(8*9)+(7*5)+(6*6)+(5*0)+(4*0)+(3*3)+(2*7)+(1*9)=175
175 % 10 = 5
So 956003-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H5BrClN/c10-8-1-2-9(11)7-5-12-4-3-6(7)8/h1-5H

956003-79-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-8-chloroisoquinoline

1.2 Other means of identification

Product number -
Other names 5-bromo-8-chloroisoquinoline

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:956003-79-5 SDS

956003-79-5Relevant articles and documents

Regioexhaustive Functionalization of the Carbocyclic Core of Isoquinoline: Concise Synthesis of Oxoaporphine Core and Ellipticine

Horváth, Dániel Vajk,Domonyi, Frigyes,Palkó, Roberta,Lomoschitz, Andrea,Soós, Tibor

, p. 2181 - 2190 (2018/03/21)

A general and versatile strategy has been developed for the functionalization of the carbocyclic core of the isoquinoline. This regioexhaustive approach employs electrophilic halogenation as a toolbox methodology and delivers highly decorated intermediates that can be further elaborated toward medicinally relevant building blocks or natural products.

ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Paragraph 0199; 0200; 0201; 0202, (2017/06/12)

A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.

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