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  2. Methanaminium,N-[(dimethylamino)[(1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)oxy]methylene]-N-methyl-, tetrafluoroborate(1-)

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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)-

Methanaminium,N-[(dimethylamino)[(1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)oxy]methylene]-N-methyl-, tetrafluoroborate(1-)

F[B-](F)(F)F.CN(C(=[O+]N1C(=O)C2C(C1=O)C1CC2C=C1)N(C)C)C Request for Quotation
Chemical Name: Methanaminium,N-[(dimethylamino)[(1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)oxy]methylene]-N-methyl-, tetrafluoroborate(1-)
CAS Number: 125700-73-4
Product Number: AG000OHW(AGN-PC-0PI3UH)
Synonyms:
MDL No:
Molecular Formula: C14H20BF4N3O3
Molecular Weight: 365.1315

Identification/Properties

Computed Properties
Molecular Weight:
365.136g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
3
Exact Mass:
365.153g/mol
Monoisotopic Mass:
365.153g/mol
Topological Polar Surface Area:
52.9A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
510
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
4
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 2-(1,3-Dioxo-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindol-2(3H)-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate serves as a valuable reagent for facilitating peptide bond formation. This complex compound acts as a coupling agent in peptide synthesis reactions, aiding in the efficient and selective formation of amide bonds between amino acid building blocks. By promoting peptide bond formation, this reagent enables the creation of complex peptide structures with high purity and yield, making it an essential tool in the field of chemical synthesis.