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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-(dimethylamino)phenyl]-1,3-thiazole-4-carboxylic acid

CN(c1ccc(cc1)c1scc(n1)C(=O)O)C Request for Quotation
Chemical Name: 2-[4-(dimethylamino)phenyl]-1,3-thiazole-4-carboxylic acid
CAS Number: 955400-50-7
Product Number: AG00H90D(AGN-PC-04GIQ8)
Synonyms:
MDL No:
Molecular Formula: C12H12N2O2S
Molecular Weight: 248.3009

Identification/Properties

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

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 2-(4-(Dimethylamino)phenyl)thiazole-4-carboxylic acid is employed as a versatile building block in chemical synthesis due to its unique structural characteristics and reactivity. This compound serves as a crucial intermediate in the synthesis of various organic compounds with diverse applications in materials science, pharmaceuticals, and agrochemicals industries. By taking advantage of the functional groups present in its structure, such as the thiazole ring and carboxylic acid moiety, chemists can efficiently modify the molecule through various chemical reactions like esterification, amidation, and nucleophilic substitutions. These transformations enable the preparation of novel derivatives and analogs with enhanced properties and biological activities, making it a valuable tool in the development of new drugs, crop protection agents, and functional materials. Furthermore, the presence of the dimethylamino group provides an opportunity for further structural diversification through derivatization or prodrug strategies, expanding the potential applications of this compound in chemical research and industrial processes.