638064
XPhos
98%
Sinônimo(s):
2-Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl
About This Item
Produtos recomendados
Nível de qualidade
Ensaio
98%
adequação da reação
reaction type: Cross Couplings
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: C-C Bond Formation
reagent type: ligand
reaction type: Heck Reaction
reagent type: ligand
reaction type: Hiyama Coupling
reagent type: ligand
reaction type: Negishi Coupling
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Stille Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling
pontuação do produto alternativo mais ecológico
old score: 2
new score: 1
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características do produto alternativo mais ecológico
Waste Prevention
Atom Economy
Use of Renewable Feedstocks
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
pf
187-190 °C (lit.)
grupo funcional
phosphine
categoria alternativa mais ecológica
cadeia de caracteres SMILES
CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1C2=C(P(C3CCCCC3)C4CCCCC4)C=CC=C2
InChI
1S/C33H49P/c1-23(2)26-21-30(24(3)4)33(31(22-26)25(5)6)29-19-13-14-20-32(29)34(27-15-9-7-10-16-27)28-17-11-8-12-18-28/h13-14,19-25,27-28H,7-12,15-18H2,1-6H3
chave InChI
UGOMMVLRQDMAQQ-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Aplicação
Direct annulation of 2-haloanilines to indoles and tryptophans catalyzed by Pd. Synthesis of regioregular polythiophenes.
For small scale and high throughput uses, product is also available as ChemBeads (928364)
On the Way Towards Greener Transition-Metal-Catalyzed Processes as Quantified by E Factors
- Preparation of functionalized benzylic sulfones via palladium-catalyzed Negishi cross-coupling between alkyl sulfones and aryl halides.
- Along with pre-milled palladium(II) acetate as a pre-catalyst for the Stille cross-coupling of aryl chlorides with tributylarylstannanes to form the corresponding biaryl compounds.
- Along with platinum chloride to catalyze the hydrosilylation of terminal arylalkynes with silanes to form functionalized β-(E)-vinylsilanes.
Informações legais
produto relacionado
Código de classe de armazenamento
13 - Non Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
Certificados de análise (COA)
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Artigos
Buchwald Phosphine Ligands
The Hazari group has developed an improved palladium precatalyst scaffold for a wide range of cross-coupling reactions
A variety of palladium-catalyzed cross-coupling reactions can be run under room temperature conditions in water with TPGS- 750-M, using a variety of commercially available palladium complexes and ligands.
Buchwald phosphine ligands for C-C, C-N, and C-O bond formation.
Protocolos
TPGS-750-M surfactant enables various reactions in water at room temperature, enhancing efficiency and versatility in synthesis.
Conteúdo relacionado
The Catalexis platform enhances catalysis by digitally optimizing catalyst selection to identify the most effective phosphine ligands for cross-coupling reactions.
A plataforma Catalexis aprimora a catálise otimizando digitalmente a seleção do catalisador para identificar os ligantes de fosfina mais eficazes para reações de acoplamento cruzado.
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