1,2,4-Triazin-3-amine, 5,6-dimethyl-


Chemical Name: 1,2,4-Triazin-3-amine, 5,6-dimethyl-
CAS Number: 17584-12-2
Product Number: AG002186(AGN-PC-0JLWM8)
Synonyms:
MDL No:
Molecular Formula: C5H8N4
Molecular Weight: 124.1438

Identification/Properties


Properties
MP:
210-212 °C(lit.);
BP:
325 °C at 760 mmHg
Storage:
Room Temperature;Light sensitive;Keep in dry area;
Form:
Solid
Refractive Index:
1.7380 (estimate)
Computed Properties
Molecular Weight:
124.147g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
124.075g/mol
Monoisotopic Mass:
124.075g/mol
Topological Polar Surface Area:
64.7A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
95
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



5,6-Dimethyl-1,2,4-triazin-3-amine, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. One of the key applications of $name$ in chemical synthesis is its role as a precursor in the synthesis of heterocyclic compounds.In organic chemistry, $name$ can be utilized as a key intermediate in the formation of complex molecules due to its unique structure and reactivity. Its triazine ring system allows for the introduction of additional functional groups, enabling chemists to tailor the properties of the final products for specific applications. Additionally, the presence of the dimethyl substituents provides steric hindrance, influencing the regioselectivity and stereoselectivity of reactions involving $name$.Moreover, 5,6-Dimethyl-1,2,4-triazin-3-amine can participate in various synthetic transformations such as acylation, alkylation, and condensation reactions. These diverse chemical reactions make $name$ a valuable tool for chemists seeking to synthesize structurally complex compounds efficiently and with high precision. By harnessing the reactivity of $name$, researchers can access a wide range of novel molecules with potential applications in drug discovery, material science, and other fields of research.