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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)-

2-Thiophenecarboxylic acid, 3-[(trifluoroacetyl)amino]-, methyl ester

COC(=O)c1sccc1NC(=O)C(F)(F)F Request for Quotation
Chemical Name: 2-Thiophenecarboxylic acid, 3-[(trifluoroacetyl)amino]-, methyl ester
CAS Number: 79128-68-0
Product Number: AG005LWA(AGN-PC-0KLE2L)
Synonyms:
MDL No:
Molecular Formula: C8H6F3NO3S
Molecular Weight: 253.1983

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
253.195g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
3
Exact Mass:
253.002g/mol
Monoisotopic Mass:
253.002g/mol
Topological Polar Surface Area:
83.6A^2
Heavy Atom Count:
16
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate is a versatile compound commonly used in chemical synthesis. As an important building block in organic chemistry, this compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and materials. Its unique structure, containing both a thiophene ring and a trifluoroacetamido group, imparts distinct properties that make it valuable in creating novel molecules with specific functions.In chemical synthesis, Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate can participate in numerous reactions to introduce functional groups, form carbon-carbon bonds, or modify existing molecules. Its trifluoroacetamido moiety provides a convenient handle for further derivatization, allowing for the introduction of diverse substituents to tailor the compound's properties. Additionally, the thiophene ring offers opportunities for aromatic substitutions, enabling the creation of compounds with enhanced aromaticity or reactivity.With its structural versatility and reactivity, Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate plays a crucial role in the design and synthesis of advanced organic compounds for various industrial applications. Its utility in chemical synthesis extends to the development of new drugs, agrochemicals with improved activity, and functional materials with tailored characteristics, making it a valuable tool for organic chemists seeking to create novel molecules for diverse purposes.