Thermo Scientific Chemicals

Phenyl phosphorodichloridate, 97%, Thermo Scientific Chemicals

Catalog number: A10479.36
500 g, Each
Thermo Scientific Chemicals

Phenyl phosphorodichloridate, 97%, Thermo Scientific Chemicals

Catalog number: A10479.36
500 g, Each
Quantity
Catalog number: A10479.36
also known as A10479-36
Price (USD)
Price: 315.00
Online price: 267.65
Your price:
Quantity
-

Chemical Identifiers

CAS
770-12-7
IUPAC Name
phenyl chlorophosphonochloridate
Molecular Formula
C6H5Cl2O2P
InChI Key
TXFOLHZMICYNRM-UHFFFAOYSA-N
SMILES
ClP(Cl)(=O)OC1=CC=CC=C1
Appearance (Color)
Clear colorless to pale yellow
Assay (GC)
≥96.0%
Refractive Index
1.5195-1.5245 @ 20?C
Identification (FTIR)
Conforms
Form
Liquid

Description

Reagent for preparation of phosphate diesters.Phenyl phosphorodichloridate is used in the preparation of symmetrical phosphate diesters. It is used as a phosphorylating agent for alcohols and amines. It is also involved in the preparation of phenylphosphoro di-(1-imidazolidate) and 2-phenyl-bis-triazoloylphosphate, which is used in peptide synthesis. It plays a vital role in the Pfitzner-Moffatt oxidation which involves oxidation of alcohols to the corresponding aldehydes and ketones. Furthermore, it is utilized in Beckmann rearrangement for the preparation of N-phenylacetamide from acetophenone oxime.

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
Reagent for preparation of phosphate diesters.Phenyl phosphorodichloridate is used in the preparation of symmetrical phosphate diesters. It is used as a phosphorylating agent for alcohols and amines. It is also involved in the preparation of phenylphosphoro di-(1-imidazolidate) and 2-phenyl-bis-triazoloylphosphate, which is used in peptide synthesis. It plays a vital role in the Pfitzner-Moffatt oxidation which involves oxidation of alcohols to the corresponding aldehydes and ketones. Furthermore, it is utilized in Beckmann rearrangement for the preparation of N-phenylacetamide from acetophenone oxime.

Solubility
Immiscible with water.

Notes
Moisture sensitive. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong bases, alcohols and strong oxidizing agents.
RUO – Research Use Only

Figures

Documents & Downloads

Certificates

    Frequently asked questions (FAQs)

    Citations & References

    Search citations by name, author, journal title or abstract text