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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)-

Boron, (benzenemethanamine)trifluoro-, (T-4)-

F[B-]([NH2+]Cc1ccccc1)(F)F Request for Quotation
Chemical Name: Boron, (benzenemethanamine)trifluoro-, (T-4)-
CAS Number: 696-99-1
Product Number: AG00FFOY(AGN-PC-0TWH7C)
Synonyms:
MDL No:
Molecular Formula: C7H9BF3N
Molecular Weight: 174.9593

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(Benzylammonio)trifluoroborate is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable source of the benzyl cation, which can participate in numerous chemical reactions to facilitate the formation of a wide range of organic compounds.One of the key applications of (Benzylammonio)trifluoroborate in chemical synthesis is in the palladium-catalyzed cross-coupling reactions. By serving as a stable and bench-stable source of the benzyl cation, this compound can be easily activated under mild reaction conditions to undergo coupling with various aryl halides or pseudohalides. This process enables the synthesis of complex organic molecules with high efficiency and selectivity.Additionally, (Benzylammonio)trifluoroborate can also be employed in the preparation of benzyl-containing reagents for further functionalization reactions. Through selective transformations of the benzyl cation derived from this compound, chemists can access a diverse array of benzyl derivatives which are crucial building blocks in organic synthesis.Overall, the unique reactivity and versatility of (Benzylammonio)trifluoroborate make it a valuable tool in modern chemical synthesis, allowing for the efficient construction of complex organic molecules with high precision and control.