Interesting facts
Interesting Facts about 2,4,6-triallyloxy-1,3,5-triazine
2,4,6-triallyloxy-1,3,5-triazine is a fascinating compound that belongs to the family of triazine derivatives, which have garnered interest in various fields, including organic chemistry and material science. Here are some noteworthy aspects of this compound:
- Chemical Structure: The molecular framework of this compound features a triazine ring, a six-membered heterocycle containing three nitrogen atoms in alternating positions. This structural arrangement contributes to its unique chemical properties.
- Versatility in Applications: Due to its functional groups, 2,4,6-triallyloxy-1,3,5-triazine can be utilized in:
- Polymer synthesis: It acts as a monomer to create polymeric materials with enhanced properties.
- Agricultural chemistry: Potential applications in agrochemicals or fertilizers can enhance crop yields.
- Medicinal chemistry: The compound and its derivatives are being explored for therapeutic uses.
- Reactivity: The presence of allyloxy groups makes this compound highly reactive, allowing for further transformations. The reactivity can be beneficial for creating complex organic molecules through:
- Cross-coupling reactions
- Radical reactions
- Research Interest: Scientists are actively investigating this compound for its properties in:
- Flame retardant materials: Its triazine structure provides a framework for developing heat-resistant materials.
- Light-absorbing materials: It is of interest for potential applications in solar energy conversion.
The compound 2,4,6-triallyloxy-1,3,5-triazine exemplifies how altering a simple molecular structure can yield a compound with a rich tapestry of functional capabilities. As research continues, the potential of this compound to impact various scientific domains remains an exciting prospect!
Synonyms
Triallyl cyanurate
101-37-1
Activator OC
2,4,6-Triallyloxy-1,3,5-triazine
Triallyl cyanaurate
Perkalink 300
Rhenofit TAC
Cyanuric acid triallyl ester
2,4,6-Tris(allyloxy)-1,3,5-triazine
Tripropargyl cyanurate
Cyanuric acid, tri-2-propenyl ester
1,3,5-Triazine, 2,4,6-tris(2-propenyloxy)-
Perkalink 300-50D
2,4,6-tris(prop-2-enoxy)-1,3,5-triazine
Rhenogran TAC/S
2,4,6-Tris(allyloxy)triazine
Rhenofit TAC/S
TAITs
2,4,6-Tri(allyloxy)-s-triazine
NSC 4804
Sartomer SR 507
s-Triazine, 2,4,6-tris(allyloxy)-
2,4,6-Tris(allyloxy)s-triazine
PLC 50BC
EINECS 202-936-7
UNII-CDD3388O1D
2,4,6-Triprop-2-ynyloxy-s-triazine
Cyanuric acid, triallyl ester
TAC-DL 70
BRN 0235560
DTXSID8037754
AI3-25448
NSC-4804
NSC-49121
SR 507
VUL-CUP TAC 70
LUVOMAXX TAC-DL 70
1,3,5-Triazine, 2,4,6-tris(2-propen-1-yloxy)-
CDD3388O1D
DTXCID6017754
EC 202-936-7
5-26-03-00532 (Beilstein Handbook Reference)
Triallyl cyanurate, stab. with 100ppm hydroquinone
2,4,6-TRIS(ALLYLOXY)-S-TRIAZINE
2,6-Tris(allyloxy)triazine
2,6-Tris(allyloxy)s-triazine
2,6-Tri(allyloxy)-s-triazine
2,6-Tris(allyloxy)-s-triazine
s-Triazine,4,6-tris(allyloxy)-
2,6-Triprop-2-ynyloxy-s-triazine
2,6-Tris(allyloxy)-1,3,5-triazine
1,5-Triazine, 2,4,6-tris(2-propenyloxy)-
WLN: T6N CN ENJ BO2U1 DO2U1 FO2U1
2,4,6-triallyloxy-1,3,5-triazi
MFCD00006049
Perkalink 30050D
SCHEMBL23181
2,4,6Tri(allyloxy)striazine
2,4,6Tris(allyloxy)triazine
2,4,6Tris(allyloxy)striazine
CHEMBL2145133
SCHEMBL16781359
NSC4804
2,4,6Triallyloxy1,3,5triazine
CHEBI:191000
Cyanuric acid, tri2propenyl ester
sTriazine, 2,4,6tris(allyloxy)
NSC49121
Tox21_300737
2,4,6Tris(allyloxy)1,3,5triazine
AKOS005207240
NCGC00163802-01
NCGC00163802-02
NCGC00254643-01
AS-15232
CAS-101-37-1
1,3,5Triazine, 2,4,6tris(2propenyloxy)
1,3,5Triazine, 2,4,6tris(2propen1yloxy)
2,4,6-Triallyloxy-1,3,5-triazine, 97%
NS00010617
T0333
E78853
A800379
Q1894083
Solubility of 2,4,6-triallyloxy-1,3,5-triazine
The solubility of 2,4,6-triallyloxy-1,3,5-triazine is an important characteristic to consider when evaluating its applications and behavior in various environments. Here are some key points to note:
Overall, understanding the solubility profile of 2,4,6-triallyloxy-1,3,5-triazine is crucial for its utilization in chemical reactions, formulations, and material science, as it dictates the method of application, processing, and the potential for interactions with other chemical species.