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1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)is a heterocyclic organic compound with the molecular formula C9H10N6. It features a triazine ring with a substituted 2,4-diamine group and a 6-(2-methylphenyl) group. This versatile chemical is widely used in the synthesis of dyes, pigments, pharmaceutical intermediates, polymers, and as a corrosion inhibitor in the oil and gas industry. It also has potential applications in materials science and organic synthesis.

30508-75-9

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30508-75-9 Usage

Uses

Used in Dye and Pigment Synthesis:
1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)is used as a key intermediate for the production of various dyes and pigments. Its unique molecular structure allows for the creation of a wide range of colors and properties, making it valuable in the textile, printing, and painting industries.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)serves as a crucial building block for the synthesis of various pharmaceutical intermediates. Its ability to form complex molecular structures makes it a valuable component in the development of new drugs and therapeutic agents.
Used in Polymer Production:
1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)is utilized as a monomer in the production of polymers. Its incorporation into polymer chains can enhance properties such as strength, stability, and resistance to environmental factors, making it useful in the manufacturing of plastics, coatings, and other materials.
Used as a Corrosion Inhibitor in Oil and Gas Industry:
In the oil and gas industry, 1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)is employed as a corrosion inhibitor. Its ability to form protective layers on metal surfaces helps prevent corrosion and extend the lifespan of pipelines, storage tanks, and other equipment.
Used in Materials Science and Organic Synthesis:
1,3,5-Triazine-2,4-diamine, 6-(2-Methylphenyl)has potential applications in the field of materials science and organic synthesis. Its unique properties and reactivity make it a promising candidate for the development of new materials and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 30508-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,0 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30508-75:
(7*3)+(6*0)+(5*5)+(4*0)+(3*8)+(2*7)+(1*5)=89
89 % 10 = 9
So 30508-75-9 is a valid CAS Registry Number.

30508-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-Methylphenyl)-1,3,5-triazine-2,4-diamine

1.2 Other means of identification

Product number -
Other names o-tolyl-pentane

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:30508-75-9 SDS

30508-75-9Downstream Products

30508-75-9Relevant academic research and scientific papers

2,4,6-trisubstituted-1,3,5-s-triazine compound and preparation and application thereof

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Paragraph 0028; 0070, (2021/10/05)

The invention provides a 2,4,6-trisubstituted-1,3,5-s-triazine compound as well as preparation and application thereof, and biguanide or dimethyl biguanide hydrochloride is used as an initial raw material to react with a cyano compound under an alkaline condition to prepare the 2,4,6-trisubstituted-1,3,5-s-triazine compound. The invention provides a simple and convenient synthetic method of a 2,4,6-trisubstituted-1,3,5-s-triazine compound, and the compound provided by the invention can be applied to preparation of an anti-myelogenous leukemia medicine, namely an enasidenib medicine. Compared with the prior art, the method for preparing the enasidenib has the advantages that two-step reaction is reduced, the use of a halogenating reagent is avoided, and the method is a green and environment-friendly chemical process. The structural formula I is shown in the specification.

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