ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate


Chemical Name: ethyl 5-bromo-2-phenyl-1,3-thiazole-4-carboxylate
CAS Number: 914347-21-0
Product Number: AG00GUNQ(AGN-PC-078TIP)
Synonyms:
MDL No:
Molecular Formula: C12H10BrNO2S
Molecular Weight: 312.1823

Identification/Properties


Computed Properties
Molecular Weight:
312.181g/mol
XLogP3:
4.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
310.962g/mol
Monoisotopic Mass:
310.962g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
271
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Thiazolecarboxylic acid, 5-bromo-2-phenyl-, ethyl ester is a versatile compound commonly utilized in chemical synthesis as a key building block. This compound plays a crucial role in the creation of various pharmaceuticals, agrochemicals, and advanced materials due to its unique structural properties and reactivity. Its specific application in organic synthesis includes the formation of important heterocyclic structures, which are essential components in the development of new drugs and crop protection agents. Additionally, this compound serves as a valuable intermediate in the preparation of custom-designed molecules with tailored properties for diverse industrial applications. In summary, the strategic incorporation of 4-Thiazolecarboxylic acid, 5-bromo-2-phenyl-, ethyl ester in chemical synthesis enables the efficient and targeted construction of complex molecular frameworks for a wide range of scientific and commercial purposes.