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3-Chloroisoquinoline-4-carbaldehyde is a chemical compound characterized by the molecular formula C10H6ClNO. It is an aldehyde derivative of the isoquinoline class, featuring a chlorine atom attached to the third carbon of the isoquinoline ring. 3-Chloroisoquinoline-4-carbaldehyde is recognized for its potential applications in various fields, including pharmaceuticals, agrochemicals, and as a fluorescent probe in chemical and biological research.

120285-29-2

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120285-29-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3-Chloroisoquinoline-4-carbaldehyde is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a valuable component in the development of new drugs and pesticides, contributing to the advancement of these industries.
Used in Chemical Research:
3-Chloroisoquinoline-4-carbaldehyde is employed as a fluorescent probe for the detection of biologically important molecules. Its ability to emit fluorescence upon interaction with specific targets makes it a valuable tool for researchers in the field of chemical biology, aiding in the discovery and study of novel molecular interactions.
Used in Biological and Pharmacological Research:
3-Chloroisoquinoline-4-carbaldehyde has been studied for its potential biological and pharmacological activities, including its role as a potential antitumor agent. Its unique chemical properties and interactions with biological systems make it a promising candidate for further research and development in the field of oncology and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 120285-29-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120285-29:
(8*1)+(7*2)+(6*0)+(5*2)+(4*8)+(3*5)+(2*2)+(1*9)=92
92 % 10 = 2
So 120285-29-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H6ClNO/c11-10-9(6-13)8-4-2-1-3-7(8)5-12-10/h1-6H

120285-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloroisoquinoline-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4-Isoquinolinecarboxaldehyde,3-chloro

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:120285-29-2 SDS

120285-29-2Downstream Products

120285-29-2Relevant academic research and scientific papers

SUBSTITUTED HETEROARYL ALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION

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Paragraph 0459; 0460, (2015/12/25)

Provided are substituted heteroaryl aldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.

SUBSTITUTED HETEROARYL ALDEHYDE COMPOUNDS AND METHODS FOR THEIR USE IN INCREASING TISSUE OXYGENATION

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Paragraph 0241, (2013/07/19)

Provided are substituted heteroaryl aldehydes and derivatives thereof that act as allosteric modulators of hemoglobin, methods and intermediates for their preparation, pharmaceutical compositions comprising the modulators, and methods for their use in treating disorders mediate by hemoglobin and disorders that would benefit from increased tissue oxygenation.

Synthesis and Reactions of Isoquinoline Derivatives II. Synthesis of 3-Chloroisoquinoline-4-aldehydes

Bartmann, W.,Konz, E.,Rueger, W.

, p. 680 - 683 (2007/10/02)

1-Aryl-substituted 1,4-dihydro-3(2H)isoquinolinones 1 are easily converted to 1-aryl-3-chloroisoquinoline-4-aldehydes 3 by a two-step procedure involving a Vilsmeier-Haack reaction followed by subsequent oxidation with potassium permanganate under acidic

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