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CS-W001157 4
Total: USD 88.00

BEHT Triflate

  • CAS No. 3075704-21-8

  • Cat. No. CS-1267464
  • Molecule weight586.52
  • Purity≥95%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

BEHT Triflate|CS-1267464

Structure of 3075704-21-8

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General Information

  • CAS No. 3075704-21-8
  • Cat. No. CS-1267464
  • Purity ≥95%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₅H₂₆F₃N₂O₇PS
  • Molecular Weight 586.52
  • Synonym(s) None
  • SMILES O=C(OCC)N(NC(OCC)=O)[P+](C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=CC=C3.O=S(C(F)(F)F)([O-])=O

Description

BEHT Triflate delivers a highly reactive trifluoromethanesulfonate leaving group paired with a sterically hindered heterocyclic scaffold, enabling efficient C–H functionalization under mild conditions. This bench-stable reagent facilitates cross-coupling reactions with high chemoselectivity and minimal side-product formation.

Application

BEHT Triflate serves as a highly effective triflating agent for the conversion of alcohols to triflate esters under mild conditions. Its bench-stable nature and excellent functional group tolerance enable reliable installation of the triflate leaving group in complex molecule synthesis. Widely employed in palladium-catalyzed cross-coupling reactions, it facilitates efficient C–C and C–heteroatom bond formation with high selectivity and minimal side reactions.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   N/A
  • LogP   N/A
  • H_Acceptors   N/A
  • H_Donors   N/A
  • Rotatable_Bonds   N/A

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