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


Chemical Name: 1,3,4-Thiadiazol-2-amine, 5-(3-methoxyphenyl)-
CAS Number: 247109-15-5
Product Number: AG002P5B(AGN-PC-0JWJCI)
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:
193
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#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



5-(3-Methoxyphenyl)-1,3,4-thiadiazol-2-amine, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure makes it an essential building block in the preparation of various pharmaceuticals, agrochemicals, and materials. In the field of medicinal chemistry, $name$ is commonly employed as a key intermediate in the synthesis of potential drug candidates due to its favorable pharmacological properties. It serves as a precursor for designing bioactive molecules targeting specific biological pathways, such as anticancer agents or antimicrobial drugs.Moreover, in the realm of materials science, the incorporation of $name$ into polymer matrices or organic frameworks enhances the material's properties, such as thermal stability or conductivity. Its presence can also impart specific functionalities to the material, making it suitable for diverse applications ranging from sensors to organic electronic devices.Overall, the significance of 5-(3-Methoxyphenyl)-1,3,4-thiadiazol-2-amine in chemical synthesis lies in its ability to facilitate the creation of novel compounds with tailored properties and functionalities, driving innovation across various scientific disciplines.