6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c]-1,2,4-triazolium tetrafluoroborate, min. 98%

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Catalog Number
ACM862095918
Product Name
6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c]-1,2,4-triazolium tetrafluoroborate, min. 98%
Structure
Structure
CAS
862095-91-8
Category
Heterocyclic Organic Compound
Synonyms
MFCD08459335; CTK8E9131; DTXSID90457105; 6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c][1,2,4]triazolium Tetrafluoroborate; CS-B0758; 6,7-Dihydro-2-pentafluorophenyl-5H-pyrrolo[2,1-c]-1,2,4-triazolium tetrafluoroborate; RT-010463; 2-(PERFLUOROPHENYL)-6,7-DIHYDRO-5H-PYRROLO[2,1-C][1,2,4]TRIAZOL-2-IUM TETRAFLUOROBORATE;
IUPAC Name
2-(2,3,4,5,6-pentafluorophenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-4-ium;tetrafluoroborate;
Molecular Weight
362.994g/mol
Molecular Formula
C11H7BF9N3;
Canonical SMILES
[B-](F)(F)(F)F.C1CC2=NN(C=[N+]2C1)C3=C(C(=C(C(=C3F)F)F)F)F;
InChI
InChI=1S/C11H7F5N3.BF4/c12-6-7(13)9(15)11(10(16)8(6)14)19-4-18-3-1-2-5(18)17-19;2-1(3,4)5/h4H,1-3H2;/q+1;-1;
InChI Key
KIWCIWCCQVTPOY-UHFFFAOYSA-N;
Application
Reagent used in the highly enantioand diastereoselective, catalytic intramolecular Stetter reaction.

Enantioselective synthesis of β-hydroxy and β-amino esters.

Organocatalytic iminium ion/carbene reaction cascade for the formation of 2,4-disubstituted cyclopentenones.

Synthesis of alloand epi-Inositol via the NHC-catalyzed carbocyclization of carbohydrate-derived dialdehydes
Complexity
349
Covalently-Bonded Unit Count
2
Exact Mass
363.059g/mol
H-Bond Acceptor
11
Heavy Atom Count
24
Monoisotopic Mass
363.059g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
21.7A^2
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