4-Thiazolecarboxylic acid, 5-amino-2-methyl-, ethyl ester


Chemical Name: 4-Thiazolecarboxylic acid, 5-amino-2-methyl-, ethyl ester
CAS Number: 31785-05-4
Product Number: AG003QC5(AGN-PC-00M2XD)
Synonyms:
MDL No:
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.2315

Identification/Properties


Properties
MP:
158-159℃
BP:
167°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
186.229g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
186.046g/mol
Monoisotopic Mass:
186.046g/mol
Topological Polar Surface Area:
93.4A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
177
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



Ethyl 5-amino-2-methylthiazole-4-carboxylate, a versatile compound, serves a crucial role in chemical synthesis as a building block for various organic molecules. In the realm of medicinal chemistry, this compound finds application in the synthesis of pharmaceuticals and biologically active compounds. Its presence in the chemical synthesis process enables the creation of diverse heterocyclic structures, providing opportunities for the development of novel drug candidates with enhanced properties. Additionally, Ethyl 5-amino-2-methylthiazole-4-carboxylate plays a significant role in the preparation of specialized materials used in industries such as agriculture, electronics, and materials science. Its strategic incorporation in synthetic pathways allows for the efficient and precise construction of complex molecular architectures, facilitating advancements in research and product development.