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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-(2-pyridinyl)-

c1ccc(nc1)c1cn2c(n1)scc2 Request for Quotation
Chemical Name: Imidazo[2,1-b]thiazole, 6-(2-pyridinyl)-
CAS Number: 96911-73-8
Product Number: AG005SH7(AGN-PC-00MKJ2)
Synonyms:
MDL No:
Molecular Formula: C10H7N3S
Molecular Weight: 201.2477

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

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-(Pyridin-2-yl)imidazo[2,1-b]thiazole is a versatile heterocyclic compound widely utilized in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and materials. This heterocyclic scaffold serves as a valuable intermediate in the synthesis of bioactive compounds due to its unique structural features and reactivity profile.In chemical synthesis, 6-(Pyridin-2-yl)imidazo[2,1-b]thiazole can be functionalized at different positions to introduce specific chemical functionalities, allowing for the generation of diverse analogs and derivatives with modified properties. Its presence in the molecular structure imparts desirable biological activities, making it an important moiety in the design of new drug candidates.Additionally, the ability of 6-(Pyridin-2-yl)imidazo[2,1-b]thiazole to participate in various synthetic transformations such as cross-coupling reactions, cyclizations, and substitution reactions further expands its utility in the development of complex molecules. Its inclusion in target molecules enhances their biological potency and selectivity, making it a valuable tool for medicinal chemists and researchers in the field of drug discovery.