(1-Pentyl)triphenylphosphonium bromide, 98%
(1-Pentyl)triphenylphosphonium bromide, 98%
(1-Pentyl)triphenylphosphonium bromide, 98%
Thermo Scientific Chemicals

(1-Pentyl)triphenylphosphonium bromide, 98%

CAS: 21406-61-1 | C23H26BrP | 413.34 g/mol
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500 g
Catalog number A12534.22
also known as A12534-22
Price (EUR)
99,30
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Quantity:
100 g
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Price (EUR)
99,30
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Chemical Identifiers
CAS21406-61-1
IUPAC Namepentyltriphenylphosphanium bromide
Molecular FormulaC23H26BrP
InChI KeyVAUKWMSXUKODHR-UHFFFAOYSA-M
SMILES[Br-].CCCCC[P+](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
Assay (Titration ex Bromide)>97.5 to <102.5%
FormCrystalline powder
Water Content (Karl Fischer Titration)<1.0%
It is used as pharmaceutical intermediates.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used as pharmaceutical intermediates.

Solubility
Partly miscible in water. Soluble in methanol and chloroform.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only

General References:

  1. L. A. Sternson.; R. Chandrasakar. Further evidence for nitrenium ion intermediacy in N-phenylhydroxylamine rearrangement to aminophenol. J. Org. Chem. 1984, 48 (22),4295-4297.
  2. Takeshi Sakamoto.; Kimio Okamoto.; Yasuo Kikugawa. Determination of configurations of N-methoxyimidoyl halides via catalytic hydrogenation. Synthesis of pure (E)-aldoximes. J. Org. Chem. 1992, 57 (11),3245-3248.