Quinazoline, 4-chloro-5,6,7,8-tetrahydro-2-(methylthio)-


Chemical Name: Quinazoline, 4-chloro-5,6,7,8-tetrahydro-2-(methylthio)-
CAS Number: 51660-11-8
Product Number: AG006UEA(AGN-PC-0L86XJ)
Synonyms:
MDL No:
Molecular Formula: C9H11ClN2S
Molecular Weight: 214.7150

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
214.711g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
214.033g/mol
Monoisotopic Mass:
214.033g/mol
Topological Polar Surface Area:
51.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
179
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



4-Chloro-2-(methylthio)-5,6,7,8-tetrahydroquinazoline, commonly referred to as $name$, serves as a versatile building block in chemical synthesis. This compound is strategically utilized in the formation of complex molecules through various synthetic pathways. In organic chemistry, $name$ is often employed as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and biologically active compounds.One of the primary applications of 4-Chloro-2-(methylthio)-5,6,7,8-tetrahydroquinazoline is its role as a precursor in the synthesis of heterocyclic compounds. By incorporating this compound into their structures, chemists can access a diverse array of molecules with unique properties and functionalities. Additionally, the presence of a chloro group and a methylthio group on the tetrahydroquinazoline scaffold allows for further derivatization, enabling the manipulation of the compound's reactivity and selectivity in subsequent reactions.Furthermore, 4-Chloro-2-(methylthio)-5,6,7,8-tetrahydroquinazoline serves as a valuable tool in medicinal chemistry research. Its structural features make it a promising candidate for designing new drug candidates or optimizing existing pharmaceuticals. By leveraging the synthetic versatility of this compound, researchers can explore novel chemical entities with potential therapeutic applications in various disease areas.In summary, the strategic utilization of 4-Chloro-2-(methylthio)-5,6,7,8-tetrahydroquinazoline in chemical synthesis enables the construction of diverse molecular architectures and facilitates the development of advanced materials and bioactive compounds. Its versatility and reactivity make it an indispensable component in the toolkit of synthetic chemists seeking to innovate in drug discovery and materials science.