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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-ethyl-4-methyl-

CCc1scc(n1)C Request for Quotation
Chemical Name: Thiazole, 2-ethyl-4-methyl-
CAS Number: 15679-12-6
Product Number: AG001P01(AGN-PC-0JKJFT)
Synonyms:
MDL No:
Molecular Formula: C6H9NS
Molecular Weight: 127.2074

Identification/Properties

Properties
BP:
173.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
127.205g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
127.046g/mol
Monoisotopic Mass:
127.046g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
74.9
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


2-Ethyl-4-methylthiazole, also known as thiazole, is a versatile compound widely utilized in chemical synthesis for its unique properties. In the realm of organic chemistry, this compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fragrance compounds. Its specific molecular structure imparts a distinctive aroma, making it a valuable ingredient in the creation of perfumes and flavoring agents. Furthermore, 2-Ethyl-4-methylthiazole is commonly employed as a precursor in the preparation of heterocyclic compounds and organic intermediates, contributing significantly to the development of novel chemical entities with diverse applications. Its role in chemical synthesis extends beyond fragrance and flavor industries, encompassing pharmaceutical research, material science, and biochemistry, highlighting its significance as a fundamental component in modern chemical processes.