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675938

Sigma-Aldrich

Me4tButylXphos

96%

Sinonimo/i:

Tetramethyl di-tBuXPhos

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About This Item

Formula empirica (notazione di Hill):
C33H53P
Numero CAS:
857356-94-6
Peso molecolare:
480.75
Numero MDL:
MFCD09038436
Codice UNSPSC:
12352002
ID PubChem:
24885309
NACRES:
NA.22

Livello qualitativo

100

Saggio

96%

Forma fisica

solid

Impiego in reazioni chimiche

reaction type: Cross Couplings
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: C-X Bond Formation

Punto di fusione

168-172 °C

Gruppo funzionale

phosphine

Stringa SMILE

CC1=C(C)C(C)=C(C)C(C(C(C(C)C)=CC(C(C)C)=C2)=C2C(C)C)=C1P(C(C)(C)C)C(C)(C)C

InChI

1S/C33H53P/c1-19(2)26-17-27(20(3)4)30(28(18-26)21(5)6)29-24(9)22(7)23(8)25(10)31(29)34(32(11,12)13)33(14,15)16/h17-21H,1-16H3
RCRYEYMHBHPZQD-UHFFFAOYSA-N

Categorie correlate

Applicazioni

Learn more about Buchwald Phosphine Ligands

Note legali

Usage subject to US Patents 6307087 and 6395916.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP5300
MKCP5194
MKCM0859
MKCJ9791
MKCG0326

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Sigma-Aldrich

804193

Me3(OMe)tBuXPhos-Pd-G3

XPhos 98%

Sigma-Aldrich

638064

XPhos

AlPhos

Sigma-Aldrich

799718

AlPhos

JackiePhos 95%

Sigma-Aldrich

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Sigma-Aldrich

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Takashi Ikawa et al.
Journal of the American Chemical Society, 129(43), 13001-13007 (2007-10-09)
We present results on the amidation of aryl halides and sulfonates utilizing a monodentate biaryl phosphine-Pd catalyst. Our results are in accord with a previous report that suggests that the formation of kappa(2)-amidate complexes is deleterious to the effectiveness of
David S Surry et al.
Chemical science, 2(1), 27-50 (2011-01-01)
Dialkylbiaryl phosphines are a valuable class of ligand for Pd-catalyzed amination reactions and have been applied in a range of contexts. This review attempts to aid the reader in the selection of the best choice of reaction conditions and ligand
Ruben Martin et al.
Accounts of chemical research, 41(11), 1461-1473 (2008-07-16)
The cores of many types of polymers, ligands, natural products, and pharmaceuticals contain biaryl or substituted aromatic structures, and efficient methods of synthesizing these structures are crucial to the work of a broad spectrum of organic chemists. Recently, Pd-catalyzed carbon-carbon
David S Surry et al.
Angewandte Chemie (International ed. in English), 47(34), 6338-6361 (2008-07-30)
Palladium-catalyzed amination reactions of aryl halides have undergone rapid development in the last 12 years, largely driven by the implementation of new classes of ligands. Biaryl phosphanes have proven to provide especially active catalysts in this context. This Review discusses

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Buchwald Ligands

Buchwald Ligands

Buchwald Phosphine Ligands

Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.

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