30863-34-4 Usage
General Description
Trimethyl 1,3,5-triazine-2,4,6-tricarboxylate, also known as melamine cyanurate, is a chemical compound commonly used as a flame retardant in various plastic and resin materials. It is a white, odorless powder that is highly stable and has a high thermal stability. When exposed to heat or flame, melamine cyanurate decomposes and releases nitrogen gas and water vapor, which helps to dilute and extinguish the fire. Due to its effectiveness in reducing the flammability of materials, melamine cyanurate is often used in the production of electronics, construction materials, and textiles to improve their fire resistance properties. Despite its flame retardant capabilities, concerns have been raised about the toxicity of melamine cyanurate, particularly in relation to its potential to release harmful gases when burned.
Check Digit Verification of cas no
The CAS Registry Mumber 30863-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,6 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30863-34:
(7*3)+(6*0)+(5*8)+(4*6)+(3*3)+(2*3)+(1*4)=104
104 % 10 = 4
So 30863-34-4 is a valid CAS Registry Number.
30863-34-4Relevant articles and documents
Synthesis of electron-deficient 1,3,5-triazines as potential azadienes for inverse-electron-demand Diels-Alder reactions
Xu, Guoxing,Zheng, Lianyou,Wang, Shixue,Dang, Qun,Bai, Xu
scheme or table, p. 361 - 369 (2010/04/02)
Various 1,3,5-triazines with electron-withdrawing groups such as esters, thioesters, and amides were prepared. These triazines were synthesized using acyl chloride coupling methods from triazine 1a and various alcohols, ethanethiol, and amines. Lowest unoccupied molecular orbital (LUMO) energy and solubility for these 1,3,5-triazines were determined to assess their potential as azadienes in inverse-electron-demand Diels-Alder reactions (IDA). The thioester 8 showed less LUMO energy and more solubility than triazine 1, suggesting that it may be a better azadiene to study triazine IDA reactions.