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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)-

methyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate

COC(=O)c1c(N)scc1c1ccc(cc1)F Request for Quotation
Chemical Name: methyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate
CAS Number: 350997-12-5
Product Number: AG00I6Y9(AGN-PC-0JVB1W)
Synonyms:
MDL No:
Molecular Formula: C12H10FNO2S
Molecular Weight: 251.2767

Identification/Properties

Computed Properties
Molecular Weight:
251.275g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
251.042g/mol
Monoisotopic Mass:
251.042g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
282
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-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-amino-4-(4-fluorophenyl)-3-thiophenecarboxylate is a versatile compound commonly utilized in the field of chemical synthesis. This particular molecule serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural composition. Through selective functional group manipulations and reactions, this compound can be tailored to introduce specific functionalities into organic molecules, enabling the synthesis of complex organic compounds with enhanced properties. Its incorporation in the synthesis of heterocyclic compounds has been particularly instrumental in the development of novel drug candidates and biologically active molecules. This compound's strategic placement within chemical synthesis pathways highlights its significance as a valuable intermediate for the production of diverse compounds with tailored properties and applications.