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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)-

Imidazo[2,1-b]thiazole, 6-methyl-

Cc1cn2c(n1)scc2 Request for Quotation
Chemical Name: Imidazo[2,1-b]thiazole, 6-methyl-
CAS Number: 3835-41-4
Product Number: AG00CZZ1(AGN-PC-0JM718)
Synonyms:
MDL No:
Molecular Formula: C6H6N2S
Molecular Weight: 138.1902

Identification/Properties

Computed Properties
Molecular Weight:
138.188g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
138.025g/mol
Monoisotopic Mass:
138.025g/mol
Topological Polar Surface Area:
45.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
118
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methylimidazo[2,1-b]thiazole is a versatile compound widely utilized in chemical synthesis as a key building block for various organic reactions. Its unique structure and reactivity make it an essential tool in the creation of complex molecules and pharmaceutical intermediates.In chemical synthesis, 6-methylimidazo[2,1-b]thiazole serves as an efficient nitrogen and sulfur-containing heterocycle, providing opportunities for the introduction of functional groups and promoting diverse transformations. Its presence in a molecule can enhance its biological activity and physical properties, making it valuable in drug discovery and development.With its ability to participate in various reactions such as cross-coupling, cyclization, and functional group modifications, 6-methylimidazo[2,1-b]thiazole enables chemists to access new chemical space and design novel compounds with specific properties. Its application extends to the synthesis of complex natural products, agrochemicals, and materials with tailored functionalities.Overall, the incorporation of 6-methylimidazo[2,1-b]thiazole in chemical synthesis offers a strategic approach to accessing diverse molecular architectures and advancing advancements in the field of organic chemistry.