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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-5-carboxaldehyde, 3,6-dimethyl-

O=Cc1c(C)nc2n1c(C)cs2 Request for Quotation
Chemical Name: Imidazo[2,1-b]thiazole-5-carboxaldehyde, 3,6-dimethyl-
CAS Number: 130182-30-8
Product Number: AG000U39(AGN-PC-0KL3G7)
Synonyms:
MDL No:
Molecular Formula: C8H8N2OS
Molecular Weight: 180.2269

Identification/Properties

Computed Properties
Molecular Weight:
180.225g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
180.036g/mol
Monoisotopic Mass:
180.036g/mol
Topological Polar Surface Area:
62.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
200
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


3,6-Dimethylimidazo[2,1-b]thiazole-5-carbaldehyde is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic chemistry, it serves as a key building block for the formation of various heterocyclic structures, particularly in the synthesis of pharmaceutically important compounds.One of the primary applications of 3,6-Dimethylimidazo[2,1-b]thiazole-5-carbaldehyde is its role as a precursor in the synthesis of biologically active molecules. Its functional groups and specific molecular structure make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, the presence of the imidazole and thiazole rings in 3,6-Dimethylimidazo[2,1-b]thiazole-5-carbaldehyde enables it to participate in a variety of synthetic transformations, such as condensation reactions, cyclizations, and cross-coupling reactions. This versatility makes it a highly sought-after compound in the field of organic synthesis.Overall, 3,6-Dimethylimidazo[2,1-b]thiazole-5-carbaldehyde plays a crucial role in the development of novel chemical entities and functional materials, showcasing its significance in advancing the frontiers of chemical science and technology.