Informativa e consenso per l'uso dei cookie

Accetto Il nostro sito salva piccoli pezzi di informazioni (cookie) sul dispositivo, al fine di fornire contenuti migliori e per scopi statistici. È possibile disattivare l'utilizzo di cookies modificando le impostazioni del tuo browser. Continuando la navigazione si acconsente all'utilizzo dei cookie.

Triphenylphosphine, polymer-supported, 1.4-2.0 mmol/g on polystyrene - L19478 - Alfa Aesar

L19478 Triphenylphosphine, polymer-supported, 1.4-2.0 mmol/g on polystyrene

Codice CAS
Sinonimi

Dimensioni Prezzo ($) Quantità Disponibilità
1g 27,52
5g 96,30
25g 350,10
Aggiungi al carrello Aggiungi al preventivo generale Visualizza articolo

Triphenylphosphine, polymer-supported, 1.4-2.0 mmol/g on polystyrene

MDL
MFCD00148025

Proprietà chimiche

Applicazioni

Triphenylphosphine is used as a support for nickel, rhenium and rhodium in hydrogenation, in dimerization of alkenes and in hydroformylation. It is also used for the halogenation of carboxylic acid and alkanes in carbon tetrachloride, addition of iodine in DMF esterifies primary and secondary alcohols to their respective formate esters and in the Mitsunobu and the Wittig reactions.

Note

Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with oxidizing agents.

Letteratura

T.A. Stephenson.; G. Wilkinson. New complexes of ruthenium (II) and (III) with triphenylphosphine, triphenylarsine, trichlorostannate, pyridine and other ligands. Journal of Inorganic and Nuclear Chemistry. 1966, 28 (4), 945-956.

Mitsuru Kato.; Masami Kamigaito.; Mitsuo Sawamoto.; Toshinobu Higashimura. Polymerization of Methyl Methacrylate with the Carbon Tetrachloride/Dichlorotris-(triphenylphosphine)ruthenium(II)/Methylaluminum Bis(2,6-di-tert-butylphenoxide) Initiating System: Possibility of Living Radical Polymerization. Macromolecules. 1995, 28 (5), 1721-1723.

Support for nickel, rhenium and rhodium in hydrogenation: J. Am. Chem. Soc., 97, 1742 (1975); dimerization of alkenes: J. Am. Chem. Soc., 97, 341 (1974) and hydroformylation: J. Am. Chem. Soc., 98 5402 (1976). For the halogenation of carboxylic acid and alkanes in carbon tetrachloride: Synthesis, 1093 (1992). Addition of iodine in DMF esterifies primary and secondary alcohols to their respective formate esters: Med. Res. Rev., 19, 97 (1999).

For use in the Mitsunobu reaction: Tetrahedron Lett., 8751 (1998), and the Wittig reaction: J. Org. Chem., 48, 326 (1983); J. Chem. Soc. Perkin 1, 2243 (1998).

Rischio GHS e dichiarazioni precauzionali

Dichiarazioni di rischio (UE): H302-H317

Harmful if swallowed. May cause an allergic skin reaction.

Dichiarazioni precauzionali: P261-P280-P264-P270-P301+P312-P363-P321-P333+P313-P302+P352-P501a

Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. Wash thoroughly after handling. Do not eat, drink or smoke when using this product. IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. Wash contaminated clothing before reuse. Specific treatment (see label). If skin irritation or rash occurs: Get medical advice/attention. IF ON SKIN: Wash with plenty of soap and water. Dispose of contents/container in accordance with local/regional/national/international regulations.

Altri riferimenti

Codice tariffe armonizzato
3903.19
TSCA
Yes

Raccomandato

  • A11284

    (3-Aminopropyl)trimethoxysilane, 97%
  • A12807

    4-Chloro-3-nitrobenzoic acid, 99%
  • A16046

    Triton® X-100
  • B22928

    trans-1,2-Diaminocyclohexane-N,N,N',N'-tetraacetic acid monohydrate, 98%
  • H27719

    1,1'-(Azodicarbonyl)dipiperidine, 97%

Visualizzati di recente

Prodotti chimici

Scienze della vita

Metalli e materiali

Catalizzatori

Apparecchiature di analisi e di laboratorio