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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)-

1,3,4-Thiadiazol-2-amine, 5-(4-methoxyphenyl)-

COc1ccc(cc1)c1nnc(s1)N Request for Quotation
Chemical Name: 1,3,4-Thiadiazol-2-amine, 5-(4-methoxyphenyl)-
CAS Number: 1014-25-1
Product Number: AG0004F0(AGN-PC-0JV0VJ)
Synonyms:
MDL No:
Molecular Formula: C9H9N3OS
Molecular Weight: 207.2523

Identification/Properties

Computed Properties
Molecular Weight:
207.251g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
207.047g/mol
Monoisotopic Mass:
207.047g/mol
Topological Polar Surface Area:
89.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
185
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(4-Methoxyphenyl)-1,3,4-thiadiazol-2-amine, commonly referred to as $name$, serves as a versatile building block in chemical synthesis. This compound exhibits remarkable reactivity and selectivity, making it a valuable tool in the creation of various pharmaceuticals, agrochemicals, and materials.One prominent application of 5-(4-Methoxyphenyl)-1,3,4-thiadiazol-2-amine is its role as a key intermediate in the synthesis of bioactive compounds. By leveraging its unique structural features, chemists can efficiently introduce functional groups and stereochemistry to design novel drug candidates with enhanced potency and selectivity.Furthermore, this compound's ability to participate in diverse chemical reactions enables the construction of complex molecular scaffolds. Through strategic modifications and derivatizations, researchers can access a wide range of structurally diverse molecules for drug discovery, material science, and other applications.In summary, the utility of 5-(4-Methoxyphenyl)-1,3,4-thiadiazol-2-amine in chemical synthesis lies in its versatility, reactivity, and ability to facilitate the construction of complex molecules with tailored properties.