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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)-

4-Thiazolecarboxylic acid, 2-(aminomethyl)-, ethyl ester

CCOC(=O)c1csc(n1)CN Request for Quotation
Chemical Name: 4-Thiazolecarboxylic acid, 2-(aminomethyl)-, ethyl ester
CAS Number: 91711-96-5
Product Number: AG00GS6U(AGN-PC-0N4IVB)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties

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


Ethyl 2-(aminomethyl)thiazole-4-carboxylate is a versatile compound that finds extensive use in chemical synthesis processes. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules.In chemical synthesis, Ethyl 2-(aminomethyl)thiazole-4-carboxylate is commonly employed as a precursor for the preparation of thiazole-based derivatives. By utilizing the amine and carboxylic acid functional groups present in the molecule, chemists can introduce various substituents and modifications to tailor the properties of the final products. This compound serves as a crucial component in the creation of bioactive compounds with potential applications in drug discovery and development.Furthermore, Ethyl 2-(aminomethyl)thiazole-4-carboxylate can undergo a range of synthetic transformations, such as condensation reactions, acylation, and cyclization processes, to yield structurally diverse molecules. Its incorporation into synthetic pathways enables chemists to access novel compounds with enhanced biological activities or specific functionalities.Overall, Ethyl 2-(aminomethyl)thiazole-4-carboxylate plays a vital role in chemical synthesis by serving as a versatile intermediate for the construction of valuable organic molecules with potential applications across various industries.