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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)-

3-Thiophenecarboxylic acid, 2-amino-4-phenyl-, methyl ester

COC(=O)c1c(N)scc1c1ccccc1 Request for Quotation
Chemical Name: 3-Thiophenecarboxylic acid, 2-amino-4-phenyl-, methyl ester
CAS Number: 67171-55-5
Product Number: AG00F9WF(AGN-PC-0JUXFS)
Synonyms:
MDL No:
Molecular Formula: C12H11NO2S
Molecular Weight: 233.2862

Identification/Properties

Computed Properties
Molecular Weight:
233.285g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
233.051g/mol
Monoisotopic Mass:
233.051g/mol
Topological Polar Surface Area:
80.6A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
253
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 2-amino-4-phenylthiophene-3-carboxylate is a versatile compound widely utilized in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique molecular structure offers opportunities for the development of novel compounds with diverse applications in the field of medicinal chemistry. By incorporating Methyl 2-amino-4-phenylthiophene-3-carboxylate into synthetic routes, chemists can efficiently access structurally complex molecules with enhanced biological activities. This compound plays a crucial role in the construction of heterocyclic frameworks, making it a valuable tool for the synthesis of biologically active molecules. Its compatibility with a wide range of synthetic methodologies highlights its significance in the synthesis of diverse chemical entities. Through strategic incorporation into synthetic pathways, Methyl 2-amino-4-phenylthiophene-3-carboxylate enables the efficient and controlled synthesis of target molecules with tailored properties and activities.