30863-34-4 Usage
Uses
Used in Plastic and Resin Materials:
Trimethyl 1,3,5-triazine-2,4,6-tricarboxylate is used as a flame retardant to enhance the fire resistance of various plastic and resin materials. Its high thermal stability and ability to decompose and release nitrogen gas and water vapor when exposed to heat or flame contribute to its effectiveness in reducing flammability.
Used in Electronics Production:
Trimethyl 1,3,5-triazine-2,4,6-tricarboxylate is used as a flame retardant in the production of electronics to improve their fire resistance properties. This helps to protect electronic devices from potential fire hazards and ensures their safety during use.
Used in Construction Materials:
Trimethyl 1,3,5-triazine-2,4,6-tricarboxylate is used as a flame retardant in the production of construction materials to enhance their fire resistance. This is particularly important in building applications where fire safety is a critical concern.
Used in Textile Industry:
Trimethyl 1,3,5-triazine-2,4,6-tricarboxylate is used as a flame retardant in the textile industry to improve the fire resistance of fabrics and other textile products. This helps to reduce the risk of fire in clothing and other textile items.
However, it is important to note that there are concerns about the toxicity of trimethyl 1,3,5-triazine-2,4,6-tricarboxylate, particularly in relation to its potential to release harmful gases when burned. This necessitates careful consideration and regulation of its use in various applications.
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 academic research and scientific papers
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.
