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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-[5-[4-(2-hydroxy-2-methylpropanoyl)piperazin-1-yl]-2-(trifluoromethyl)phenyl]-4-(1H-indol-3-yl)pyrrole-2,5-dione

O=C(C(O)(C)C)N1CCN(CC1)c1ccc(c(c1)C1=C(C(=O)NC1=O)c1c[nH]c2c1cccc2)C(F)(F)F Request for Quotation
Chemical Name: 3-[5-[4-(2-hydroxy-2-methylpropanoyl)piperazin-1-yl]-2-(trifluoromethyl)phenyl]-4-(1H-indol-3-yl)pyrrole-2,5-dione
CAS Number: 1260181-14-3
Product Number: AG009FP5(AGN-PC-08WI1L)
Synonyms:
MDL No:
Molecular Formula: C27H25F3N4O4
Molecular Weight: 526.5070

Identification/Properties

Computed Properties
Molecular Weight:
526.516g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
4
Exact Mass:
526.183g/mol
Monoisotopic Mass:
526.183g/mol
Topological Polar Surface Area:
106A^2
Heavy Atom Count:
38
Formal Charge:
0
Complexity:
1000
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


TCS-21311 is a versatile chemical reagent commonly used in organic synthesis as a powerful catalyst for various transformations. Its excellent selectivity and reactivity make it a valuable tool for chemists seeking to efficiently and selectively create complex molecules. In chemical synthesis, TCS-21311 can facilitate a range of reactions, including carbon-carbon bond formations, dehydrogenations, oxidations, and reductions. Its unique properties enable precise control over reaction conditions, leading to high yields and minimal byproducts. Chemists often rely on TCS-21311 to streamline synthetic pathways, accelerate reaction rates, and access novel chemical structures with high efficiency.