(tert-Butoxycarbonylmethylene)triphenylphosphorane, 98%
(tert-Butoxycarbonylmethylene)triphenylphosphorane, 98%
(tert-Butoxycarbonylmethylene)triphenylphosphorane, 98%
Thermo Scientific Chemicals

(tert-Butoxycarbonylmethylene)triphenylphosphorane, 98%

CAS: 35000-38-5 | C24H25O2P | 376.44 g/mol
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Quantity:
5 g
25 g
Catalog number L15144.06
also known as L15144-06
Price (EUR)
76,80
Each
Quantity:
5 g
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Price (EUR)
76,80
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Chemical Identifiers
CAS35000-38-5
IUPAC Nametert-butyl 2-(triphenyl-λ⁵-phosphanylidene)acetate
Molecular FormulaC24H25O2P
InChI KeyZWZUFQPXYVYAFO-UHFFFAOYSA-N
SMILESCC(C)(C)OC(=O)C=P(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (HPLC)≥97.5%
Appearance (Color)White to pale yellow
FormCrystals or powder or crystalline powder
(tert-Butoxycarbonylmethylene)triphenylphosphorane is a chemical used in the synthesis of aldose reductase inhibitors, a podophyllotoxin derivative and tautomycin, a podophyllotoxin derivative and tautomycin. It Is also used in medicinal chemistry.

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
(tert-Butoxycarbonylmethylene)triphenylphosphorane is a chemical used in the synthesis of aldose reductase inhibitors, a podophyllotoxin derivative and tautomycin, a podophyllotoxin derivative and tautomycin. It Is also used in medicinal chemistry.

Solubility
Sparingly soluble in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature is 2 - 8°C. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. B L Mylari.; W J Zembrowski.; T A Beyer, C E Aldinger.; T W Siegel. Orally active aldose reductase inhibitors: indazoleacetic, oxopyridazineacetic, and oxopyridopyridazineacetic acid derivatives. Langmuir. 1992, 35 (12), 2155-2162.
  2. Rabindra Rej.; Dieu Nguyen.; Brian Go.; Samuel Fortin.; Jean-François Lavallée. Total Synthesis of Cryptophycins and Their 16-(3-Phenylacryloyl) Derivatives. J. Org. Chem. 1996, 61 (18), 6289-6295.