Imidazo[2,1-b]thiazole-3-carboxylic acid, 6-(2-nitrophenyl)-, ethyl ester


Chemical Name: Imidazo[2,1-b]thiazole-3-carboxylic acid, 6-(2-nitrophenyl)-, ethyl ester
CAS Number: 925437-84-9
Product Number: AG0064FW(AGN-PC-04XWX7)
Synonyms:
MDL No:
Molecular Formula: C14H11N3O4S
Molecular Weight: 317.3198

Identification/Properties


Properties
Form:
Solid
Computed Properties
Molecular Weight:
317.319g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
4
Exact Mass:
317.047g/mol
Monoisotopic Mass:
317.047g/mol
Topological Polar Surface Area:
118A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
444
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate, a versatile compound in chemical synthesis, serves as a valuable building block for the creation of various organic molecules. It is widely used in pharmaceutical and agrochemical industries for the preparation of novel drug candidates and pesticides due to its unique structural features. The presence of an imidazole ring, nitrophenyl group, and thiazole core in this compound offers a wide range of reactivity, making it an essential moiety in the construction of diverse molecular scaffolds. Its application in the synthesis of heterocyclic compounds, coordination complexes, and biologically active molecules highlights its significance in modern organic chemistry research.