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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-(3,5-dimethylphenyl)-1,3-thiazole-4-carbaldehyde

O=Cc1csc(n1)c1cc(C)cc(c1)C Request for Quotation
Chemical Name: 2-(3,5-dimethylphenyl)-1,3-thiazole-4-carbaldehyde
CAS Number: 885278-96-6
Product Number: AG00459H(AGN-PC-09RR2L)
Synonyms:
MDL No:
Molecular Formula: C12H11NOS
Molecular Weight: 217.2868

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
217.286g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
217.056g/mol
Monoisotopic Mass:
217.056g/mol
Topological Polar Surface Area:
58.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
224
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


The compound 2-(3,5-Dimethylphenyl)-4-thiazolecarboxaldehyde plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing both a thiazole ring and an aldehyde functional group makes it a valuable intermediate in the preparation of various complex organic molecules. In chemical synthesis, this compound can be used as a key starting material for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The aldehyde group provides a site for further functionalization through various reactions, allowing for the introduction of different chemical functionalities. Additionally, the presence of the thiazole ring confers specific properties to the molecule, which can be exploited for designing new compounds with desired biological or physicochemical activities. Overall, the application of 2-(3,5-Dimethylphenyl)-4-thiazolecarboxaldehyde in chemical synthesis enables the efficient construction of diverse organic compounds with potential applications in various industries.