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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)-

2,4-dibromo-5-methyl-1,3-thiazole

Brc1sc(c(n1)Br)C Request for Quotation
Chemical Name: 2,4-dibromo-5-methyl-1,3-thiazole
CAS Number: 1206708-88-4
Product Number: AG003FPL(AGN-PC-0HAOBQ)
Synonyms:
MDL No: MFCD23135672
Molecular Formula: C4H3Br2NS
Molecular Weight: 256.9463

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
256.943g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
256.833g/mol
Monoisotopic Mass:
254.835g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
90.1
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


2,4-Dibromo-5-methylthiazole is a versatile compound that finds widespread application in chemical synthesis as a key building block. This unique molecule serves as a valuable intermediate in the development of various pharmaceuticals, agrochemicals, and materials due to its structural attributes and reactivity. In organic synthesis, 2,4-Dibromo-5-methylthiazole can participate in cross-coupling reactions, Suzuki-Miyaura couplings, and other transformations to create complex molecular structures with potential biological activities. Its functional groups facilitate the introduction of diverse side chains or substituents, allowing for the modification of properties and functionalities in target molecules. Additionally, the thiazole ring system in 2,4-Dibromo-5-methylthiazole imparts desirable physicochemical properties that can enhance the efficacy or performance of the final products. As a key player in the realm of chemical synthesis, this compound enables chemists to access a wide array of structurally diverse compounds with tailored properties for various applications in medicinal chemistry, materials science, and beyond.