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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)-

Methanone, (2-amino-4,5-dimethyl-3-thienyl)[3-(trifluoromethyl)phenyl]-

Nc1sc(c(c1C(=O)c1cccc(c1)C(F)(F)F)C)C Request for Quotation
Chemical Name: Methanone, (2-amino-4,5-dimethyl-3-thienyl)[3-(trifluoromethyl)phenyl]-
CAS Number: 132861-87-1
Product Number: AG00119K(AGN-PC-0JLNSO)
Synonyms:
MDL No:
Molecular Formula: C14H12F3NOS
Molecular Weight: 299.3114

Identification/Properties

Computed Properties
Molecular Weight:
299.311g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
2
Exact Mass:
299.059g/mol
Monoisotopic Mass:
299.059g/mol
Topological Polar Surface Area:
71.3A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
374
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


($name$) is a versatile compound that is frequently utilized in chemical synthesis as a key building block. Its unique structure allows for the introduction of both amino and carbonyl functionalities, making it a valuable intermediate in the creation of complex organic molecules. Specifically, ($name$) is commonly employed as a reagent in the formation of heterocyclic compounds, pharmaceuticals, and agrochemicals. Its involvement in chemical transformations such as cyclization reactions, cross-coupling processes, and functional group manipulations highlights its significance in the development of novel synthetic methodologies. In addition, the presence of the trifluoromethylphenyl group in ($name$) imparts desirable properties such as enhanced reactivity and selectivity, further expanding its utility in diverse synthetic applications.