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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)-

3H-1,2,4-Triazole-3-thione, 4-amino-2,4-dihydro-5-(3-pyridinyl)-

Nn1c(S)nnc1c1cccnc1 Request for Quotation
Chemical Name: 3H-1,2,4-Triazole-3-thione, 4-amino-2,4-dihydro-5-(3-pyridinyl)-
CAS Number: 78027-00-6
Product Number: AG008NRF(AGN-PC-0JX1VR)
Synonyms:
MDL No:
Molecular Formula: C7H7N5S
Molecular Weight: 193.2290

Identification/Properties

Computed Properties
Molecular Weight:
193.228g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
193.042g/mol
Monoisotopic Mass:
193.042g/mol
Topological Polar Surface Area:
98.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
251
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


4-Amino-5-(pyridin-3-yl)-4H-1,2,4-triazole-3-thiol, also known as $name$, is a versatile compound with significant applications in chemical synthesis. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and materials due to its unique structural properties. In chemical synthesis, $name$ is commonly used as a building block or intermediate in the preparation of various biologically active molecules. Its functional groups allow for selective modifications and transformations, making it a valuable tool for the synthesis of complex organic compounds. Additionally, the presence of the thiol group in $name$ enables it to participate in a variety of chemical reactions, such as nucleophilic addition, substitution, and metal complexation. This reactivity broadens its utility in the creation of novel chemical structures and functional materials.Overall, the versatility of 4-Amino-5-(pyridin-3-yl)-4H-1,2,4-triazole-3-thiol makes it a valuable component in the toolbox of synthetic chemists, facilitating the exploration of new chemical entities with potential applications in various fields.