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Merck
CN

673951

Tricyclopentylphosphine tetrafluoroborate

greener alternative

95%

Synonym(s):

Cyp3HBF4, PCyp3HBF4

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About This Item

Empirical Formula (Hill Notation):
C15H28BF4P
CAS Number:
610756-04-2
Molecular Weight:
326.16
UNSPSC Code:
12352101
PubChem Substance ID:
24885190
MDL number:
MFCD08705305

Key Documents

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Product Name

Tricyclopentylphosphine tetrafluoroborate, 95%

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

SMILES string

F[B-](F)(F)F.C1CCC(C1)[PH+](C2CCCC2)C3CCCC3

InChI key

KTDMVANQORSVPI-UHFFFAOYSA-O

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

Application

Catalyst for alkane C-H arylation from aryl chlorides
Ligand for ruthenium-catalyzed greener amide bond formation by dehydrogenative coupling of amines and alcohols.

Amide Synthesis from Alcohols and Amines by the Extrusion of Dihydrogen
Used with Ru(cod)Cl dimer to catalyze the dehydrogenative coupling of alcohols and amines to form amide bonds.

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
15507DE

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Protocols

Bestmann-Ohira Reagent: Alkynes from Aldehydes

Acetylene chemistry's versatile applications from organic synthesis to bioorganic chemistry demand efficient synthesis methods.

Bestmann-Ohira 试剂：从醛类协议合成炔烃

乙炔化学一直是并且仍然是分子科学的重要组成部分。它的潜力和广泛的应用从有机合成到材料科学再到生物有机化学。一些例子是烯二炔（DNA切割剂），“点击化学”工具和构建块。 因此，它引发了对高效合成炔烃的需求。

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