Thermo Scientific Chemicals

Burgess Reagent, 96%

Catalog number: L20155.03
1 g, Each
Thermo Scientific Chemicals

Burgess Reagent, 96%

Catalog number: L20155.03
1 g, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: L20155.03
also known as L20155-03
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Chemical Identifiers

CAS
29684-56-8
IUPAC Name
(methoxycarbonyl)[(triethylazaniumyl)sulfonyl]azanide
Molecular Formula
C8H18N2O4S
InChI Key
YSHOWEKUVWPFNR-UHFFFAOYSA-N
SMILES
CC[N+](CC)(CC)S(=O)(=O)[N-]C(=O)OC
Form
Crystals or powder or crystalline powder or lumps
Appearance (Color)
White to cream to yellow
Assay (HPLC)
≥95.0%
Identification (FTIR)
Conforms

Description

Burgess reagent is a selective dehydrating reagent used in organic synthesis. It is used to convert secondary and tertiary alcohol, with an adjacent proton, into alkenes. Burgess reagent is also utilized to promote great synthetic values in medicinal chemistry. It has been used in dehydration of primary amides, formamides and primary nitroalkanes to generate nitriles, isocyanides and nitrile oxides respectively. It forms urethanes when it reacts with primary alcohols.

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
Burgess reagent is a selective dehydrating reagent used in organic synthesis. It is used to convert secondary and tertiary alcohol, with an adjacent proton, into alkenes. Burgess reagent is also utilized to promote great synthetic values in medicinal chemistry. It has been used in dehydration of primary amides, formamides and primary nitroalkanes to generate nitriles, isocyanides and nitrile oxides respectively. It forms urethanes when it reacts with primary alcohols.

Solubility
Soluble in organic solvents.

Notes
Store in cool place. Moisture sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only

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