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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)-

Methanesulfonamide,N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[1,1,1-trifluoro-

FC(S(=O)(=O)N[C@H]([C@H](c1ccccc1)NS(=O)(=O)C(F)(F)F)c1ccccc1)(F)F Request for Quotation
Chemical Name: Methanesulfonamide,N,N'-[(1S,2S)-1,2-diphenyl-1,2-ethanediyl]bis[1,1,1-trifluoro-
CAS Number: 121788-77-0
Product Number: AG00161C(AGN-PC-0PFS28)
Synonyms:
MDL No:
Molecular Formula: C16H14F6N2O4S2
Molecular Weight: 476.4138

Identification/Properties

Properties
BP:
484.6°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
476.408g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
12
Rotatable Bond Count:
7
Exact Mass:
476.03g/mol
Monoisotopic Mass:
476.03g/mol
Topological Polar Surface Area:
109A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
694
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N'-((1S,2S)-1,2-diphenylethane-1,2-diyl)bis(1,1,1-trifluoromethanesulfonamide) is a versatile compound utilized in chemical synthesis as a powerful reagent for various transformations. Its application extends to asymmetric synthesis, where it acts as a chiral source in catalytic reactions, allowing for the selective formation of enantiopure products. This compound is particularly valuable in the preparation of pharmaceutical intermediates and natural product synthesis, where stereochemical control is crucial. Additionally, it can serve as a building block for designing new ligands or catalysts in organometallic chemistry, enabling the creation of complex molecular structures with high precision. In summary, the compound plays a pivotal role in enabling synthetic chemists to access challenging structural motifs with high levels of stereo- and regioselectivity.