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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1,2,4-Triazine-3(2H)-thione, 5,6-diphenyl-

Sc1nnc(c(n1)c1ccccc1)c1ccccc1 Request for Quotation
Chemical Name: 1,2,4-Triazine-3(2H)-thione, 5,6-diphenyl-
CAS Number: 37469-24-2
Product Number: AG00C8BC(AGN-PC-0JV4WM)
Synonyms:
MDL No:
Molecular Formula: C15H11N3S
Molecular Weight: 265.3329

Identification/Properties

Computed Properties
Molecular Weight:
265.334g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
265.067g/mol
Monoisotopic Mass:
265.067g/mol
Topological Polar Surface Area:
68.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
402
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Mercapto-5,6-diphenyl-1,2,4-triazine holds a crucial role in chemical synthesis as a versatile building block. Its application in organic chemistry is well-known for its ability to act as a key intermediate in the creation of various compounds. Due to its unique structure and reactivity, this compound serves as a valuable tool in the formation of complex molecules with diverse functionalities.One significant use of 3-Mercapto-5,6-diphenyl-1,2,4-triazine is in the synthesis of heterocyclic compounds, where it can participate in cyclization reactions to form ring structures. This compound's thiol group enables it to engage in various types of reactions, such as nucleophilic substitution and addition reactions, leading to the formation of new bonds and functional groups. Additionally, its presence as a triazine moiety enhances its versatility in coupling reactions, enabling the attachment of other molecules or groups to generate elaborate structures.Furthermore, 3-Mercapto-5,6-diphenyl-1,2,4-triazine's role in chemical synthesis extends to pharmaceutical and material science applications. Its presence as a sulfur-containing heterocycle imparts unique properties to the synthesized compounds, making them potential candidates for drug discovery or materials development. By incorporating this compound into the design of target molecules, chemists can access a diverse array of compounds with tailored properties and functionalities.In summary, 3-Mercapto-5,6-diphenyl-1,2,4-triazine serves as a valuable tool in chemical synthesis, offering a wide range of possibilities for creating novel compounds in organic chemistry. Its reactivity, versatility, and unique structural features make it a key component in the toolbox of synthetic chemists, enabling the construction of intricate molecules with specific applications in various fields of research and industry.