3-Thiophenecarboxylic acid, 2-amino-4-(4-fluorophenyl)-, ethyl ester


Chemical Name: 3-Thiophenecarboxylic acid, 2-amino-4-(4-fluorophenyl)-, ethyl ester
CAS Number: 35978-33-7
Product Number: AG003Q30(AGN-PC-0JTSRZ)
Synonyms:
MDL No:
Molecular Formula: C13H12FNO2S
Molecular Weight: 265.3033

Identification/Properties


Properties
MP:
92-95 °C
BP:
388.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
265.302g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
265.057g/mol
Monoisotopic Mass:
265.057g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
295
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:
H315-H319-H335
Precautionary Statements:
P261-P280-P305+P351+P338-P304+P340-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



Ethyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate is a versatile chemical compound that finds application in various chemical synthesis processes. It serves as a key building block in the creation of pharmaceuticals, agrochemicals, and organic materials. This compound is particularly prized for its role in the synthesis of heterocyclic compounds, which are essential in drug development and materials science. With its unique chemical structure, Ethyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate enables the formation of complex molecules with specific properties and functions, making it an indispensable tool for synthetic chemists in the pursuit of innovative advancements in various fields.