673951
Tricyclopentylphosphine tetrafluoroborate
95%
Synonym(s):
Cyp3HBF4, PCyp3HBF4
About This Item
Recommended Products
Assay
95%
form
solid
reaction suitability
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
reaction type: Cross Couplings
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
246-264 °C
functional group
phosphine
greener alternative category
, Aligned
SMILES string
F[B-](F)(F)F.C1CCC(C1)[PH+](C2CCCC2)C3CCCC3
InChI
1S/C15H27P.BF4/c1-2-8-13(7-1)16(14-9-3-4-10-14)15-11-5-6-12-15;2-1(3,4)5/h13-15H,1-12H2;/q;-1/p+1
InChI key
KTDMVANQORSVPI-UHFFFAOYSA-O
General description
Application
Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Protocols
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Acetylene chemistry's versatile applications from organic synthesis to bioorganic chemistry demand efficient synthesis methods.
Acetylene chemistry's versatile applications from organic synthesis to bioorganic chemistry demand efficient synthesis methods.
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