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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)-

ethyl 2,5-dichloro-1,3-thiazole-4-carboxylate

CCOC(=O)c1nc(sc1Cl)Cl Request for Quotation
Chemical Name: ethyl 2,5-dichloro-1,3-thiazole-4-carboxylate
CAS Number: 135925-33-6
Product Number: AG009WO1(AGN-PC-003PR0)
Synonyms:
MDL No:
Molecular Formula: C6H5Cl2NO2S
Molecular Weight: 226.0804

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


Ethyl 2,5-dichloro-4-thiazolecarboxylate is a versatile compound widely used in chemical synthesis for its valuable applications. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. Its ability to undergo diverse chemical transformations makes it a crucial intermediate in the production of complex organic molecules. In particular, Ethyl 2,5-dichloro-4-thiazolecarboxylate plays a significant role in the development of novel therapeutic agents, insecticides, and other specialized chemicals. Its presence in chemical reactions facilitates the creation of new chemical entities with improved properties and functionalities, thus contributing to advancements in the field of organic chemistry. Through strategic incorporation into synthetic routes, Ethyl 2,5-dichloro-4-thiazolecarboxylate enables the generation of structurally diverse compounds with tailored characteristics, making it an indispensable component in modern chemical synthesis strategies.