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1805783-60-1

1805783-60-1 Structure

1805783-60-1 Structure
IdentificationBack Directory
[Name]

[4''-Butyl-2'',3'',5'',6''-tetrafluoro-3-methoxy-2',4',6'-tris(1-methylethyl)[1,1':3',1''-terphenyl]-2-yl]bis(tricyclo[3.3.1.1(3,7)]dec-1-yl)phosphine
[CAS]

1805783-60-1
[Synonyms]

6-Methoxy-2-{2,4,6-tri-i-propyl-3-[(2,3,5,6-tetrafluoro-4-butyl )phenyl]phenyl}diadamantyl phosphine, 98%
6-Methoxy-2-{2,4,6-tri-i-propyl-3-[(2,3,5,6-tetrafluoro-4-butyl )phenyl]phenyl}diadamantyl phosphine, 98% AlPhos
[4''-Butyl-2'',3'',5'',6''-tetrafluoro-3-methoxy-2',4',6'-tris(1-methylethyl)[1,1':3',1''-terphenyl]-2-yl]bis(tricyclo[3.3.1.1(3,7)]dec-1-yl)phosphine
[Molecular Formula]

C52H67F4OP
[MDL Number]

MFCD29905023
[MOL File]

1805783-60-1.mol
[Molecular Weight]

815.06
Chemical PropertiesBack Directory
[Melting point ]

218-223 °C
[form ]

Powder
[color ]

white to yellow
[Sensitive ]

air sensitive
[InChIKey]

ALWIRDZSIXWCBO-UHFFFAOYSA-N
[SMILES]

P(C1=C(OC)C=CC=C1C1=C(C(C)C)C=C(C(C)C)C(C2=C(F)C(F)=C(CCCC)C(F)=C2F)=C1C(C)C)(C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2
Questions And AnswerBack Directory
[Reaction]

  1. Ligand for the Palladium-Catalyzed Fluorination of Five-Membered Heteroaryl Bromides
  2. Ligand for the Palladium-Catalyzed Fluorination of Aryl Triflates and Bromides
Reactions of 1805783-60-1
Hazard InformationBack Directory
[General Description]

AlPhos is a versatile, highly efficient ligand used extensively in various important organic transformations. Recognized for its unique structure and attributes, AlPhos serves as an impressive catalyst that enables several key synthetic processes. It is primarily used in the following coupling reactions: Buchwald-Hartwig cross coupling, Suzuki-Miyaura coupling, Stille coupling, Sonogashira coupling, Negishi coupling, Heck coupling, Hiyama coupling reaction. With its remarkable performance across these reactions, AlPhos represents an invaluable tool in preparing and producing pharmaceuticals, agrochemicals, and polymers.
[Uses]

AlPhos is used in the selective arylation of aminophenylalanine in unprotected peptides with organometallic palladium reagents.
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