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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)-

Thiazole, 2-methyl-4-phenyl-

Cc1scc(n1)c1ccccc1 Request for Quotation
Chemical Name: Thiazole, 2-methyl-4-phenyl-
CAS Number: 1826-16-0
Product Number: AG002400(AGN-PC-0JTAW6)
Synonyms:
MDL No:
Molecular Formula: C10H9NS
Molecular Weight: 175.2502

Identification/Properties

Computed Properties
Molecular Weight:
175.249g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
175.046g/mol
Monoisotopic Mass:
175.046g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-4-phenylthiazole is a versatile compound widely used in chemical synthesis as a key building block for the creation of various pharmaceuticals and agrochemicals. It serves as a valuable intermediate in the production of thiazole-based drugs due to its unique structural properties, including its aromatic ring system and sulfur-containing heterocycle.In chemical synthesis, 2-Methyl-4-phenylthiazole is utilized as a precursor for the synthesis of complex molecules with therapeutic applications. Its incorporation into drug molecules can impart desirable pharmacological activities, such as antimicrobial, antifungal, and anticancer properties. By functionalizing the thiazole ring of 2-Methyl-4-phenylthiazole with different substituents, chemists can tailor the compound's reactivity and specificity to target specific biological pathways or molecular targets.Additionally, 2-Methyl-4-phenylthiazole can be employed in the development of new materials, such as dyes and pigments, due to its aromatic nature and potential for color properties. Its ability to participate in various chemical reactions, such as condensation, oxidation, and halogenation, makes it a valuable tool for synthetic chemists seeking to design novel compounds for diverse applications.Overall, the application of 2-Methyl-4-phenylthiazole in chemical synthesis offers a wide range of possibilities for the creation of innovative molecules with important biological activities and material properties.