29366-76-5 Usage
General Description
6-(3-Methylphenyl)-1,3,5-triazine-2,4-diamine, also known as Melamine, is a chemical compound with the molecular formula C 6 H 9 N 3 . It is a white crystalline solid that is commonly used in the production of plastics, adhesives, and flame retardants. Melamine is also used in the manufacturing of kitchenware and tableware due to its durability and heat-resistant properties. Additionally, it is utilized as a fertilizer and in the production of paper and textiles. However, melamine has been the subject of controversy due to its presence in certain food products and its potential health hazards when consumed in high quantities.
Check Digit Verification of cas no
The CAS Registry Mumber 29366-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,6 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 29366-76:
(7*2)+(6*9)+(5*3)+(4*6)+(3*6)+(2*7)+(1*6)=145
145 % 10 = 5
So 29366-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N5/c1-6-3-2-4-7(5-6)8-13-9(11)15-10(12)14-8/h2-5H,1H3,(H4,11,12,13,14,15)
29366-76-5Relevant articles and documents
2,4,6-trisubstituted-1,3,5-s-triazine compound and preparation and application thereof
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Paragraph 0028; 0057, (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.