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1-Isoquinolinamine,6-methyl-(9CI), also known as 6-Methylisoquinoline, is a chemical compound with the molecular formula C10H11N. It is a derivative of isoquinoline, featuring a methyl group at the 6th position. 1-Isoquinolinamine,6-methyl-(9CI) is a yellowish-brown solid at room temperature and exhibits sparing solubility in water. Its versatile nature and potential for various applications make it a compound of interest to researchers across different scientific disciplines.

42398-74-3

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42398-74-3 Usage

Uses

Used in Organic Synthesis:
1-Isoquinolinamine,6-methyl-(9CI) is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows it to be a valuable component in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new and effective compounds in these fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-Isoquinolinamine,6-methyl-(9CI) is used as a precursor for the synthesis of various pharmaceuticals. Its structural properties make it suitable for the development of new drugs, potentially leading to advancements in the treatment of various diseases and conditions.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 1-Isoquinolinamine,6-methyl-(9CI) is utilized as a precursor for the synthesis of agrochemicals. Its application in this field can contribute to the development of new pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Used in Materials Science:
1-Isoquinolinamine,6-methyl-(9CI) also has potential applications in the field of materials science. Its unique properties can be harnessed to develop new materials with specific characteristics, such as conductivity, magnetism, or optical properties, which can be useful in various technological applications.
Used as a Ligand in Coordination Chemistry:
Furthermore, 1-Isoquinolinamine,6-methyl-(9CI) can be used as a ligand in coordination chemistry. Its ability to form coordination complexes with metal ions can lead to the development of new catalysts, sensors, or materials with unique properties, expanding the scope of its applications in various scientific and industrial fields.

Check Digit Verification of cas no

The CAS Registry Mumber 42398-74-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,9 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42398-74:
(7*4)+(6*2)+(5*3)+(4*9)+(3*8)+(2*7)+(1*4)=133
133 % 10 = 3
So 42398-74-3 is a valid CAS Registry Number.

42398-74-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methylisoquinolin-1-amine

1.2 Other means of identification

Product number -
Other names 6-methyl-isoquinolin-1-ylamine

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:42398-74-3 SDS

42398-74-3Upstream product

42398-74-3Downstream Products

42398-74-3Relevant academic research and scientific papers

Method for synthesizing 1-aminoisoquinoline skeleton by rhodium-catalyzed 4-phenyl oxadiazolone and vinylene carbonate

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Paragraph 0012-0013, (2021/12/07)

The invention discloses a method for generating 1-aminoisoquinoline and a derivative thereof through a rhodium-catalyzed reaction of a 4-phenyl oxadiazolone compound and vinylene carbonate. According to the invention, a 4-phenyl oxadiazolone compound is used as a raw material and reacts with vinylene carbonate under the catalysis of transition metal rhodium to generate an isoquinoline ring. The synthesis operation steps are simple, the atom economy is high, the application range of the substrate is wide, the post-treatment operation is simpler, the implementation feasibility is high, and a foundation is laid for industrial production and wide application of the aminoisoquinoline compound.

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