Tetraphenylphosphonium Chloride Suppliers USA
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Tetraphenylphosphonium Chloride Quick inquiry Where to buy Suppliers range | Tetraphenylphosphonium Chloride. Uses: Tetraphenylphosphonium chloride is used to generate lipophilic salts from inorganic and organometallic anions. Thus, Ph4P+ is useful as a phase-transfer catalyst, again because it allows inorganic anions to dissolve in organic solvents. Depending on the size of the alkyl groups, the reaction of tetraphenylphosphonium chloride with a lithium dialkylamide can proceed in two directions to give 9-phenyl-9-phosphafluorene and benzene, or triphenylphosphine and the dialkylaniline. Lithium monoalkylamides react with tetraphenylphosphonium chloride to give (also depending on the size of the substituents) either N-alkyltriphenylphosphines or phosphine. Group: Heterocyclic Organic Compound. Alternative Names: Tetraphenylphosphonium chloride, for the spectrophotometric det. of Bi, Co, >=97.0%; C-21234; tetraphenylphophonium chloride; tetraphenylphosphanium,chloride; WAGFXJQAIZNSEQ-UHFFFAOYSA-M; Tetraphenylphosphonium chloride, 98%; KS-000001IL; ST24031894; O459; I01-1008. CAS No. 2001-45-8. Molecular formula: C24H20ClP. Mole weight: 374.848g/mol. IUPAC Name: tetraphenylphosphanium;chloride. Rotatable Bond Count: 4. Exact Mass: 374.099g/mol. EC Number: 217-890-3. SMILES: C1=CC=C (C=C1)[P+] (C2=CC=CC=C2) (C3=CC=CC=C3)C4=CC=CC=C4. [Cl-]. InChI: InChI=1S/C24H20P.ClH/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;1H/q+1;/p-1. InChIKey: WAGFXJQAIZNSEQ-UHFFFAOYSA-M. H-Bond Acceptor: 1. Monoisotopic Mass: 374.099g/mol. |