Benzaldehyde p-Toluenesulfonylhydrazone

>98.0%(HPLC)

Reagent Code: #59644
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CAS Number 1666-17-7

science Other reagents with same CAS 1666-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.34 g/mol
Formula C₁₄H₁₄N₂O₂S
badge Registry Numbers
MDL Number MFCD00009644
thermostat Physical Properties
Melting Point 130°C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Benzaldehyde p-toluenesulfonylhydrazone is a key reagent and intermediate in organic synthesis, particularly in the Shapiro reaction for regioselective formation of alkenes via vinyllithium intermediates and in the Bamford-Stevens reaction for generating diazoalkanes and carbenes. It is widely used in the preparation of heterocyclic compounds and other nitrogen-containing structures valuable for pharmaceuticals and agrochemicals. The compound facilitates studies of reaction mechanisms involving carbon-nitrogen bond formation/breaking and nitrogen extrusion. In analytical chemistry, it serves as a derivatization agent for detecting and quantifying carbonyl compounds.

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Test Parameter Specification
Appearance White to pale yellow solid
Purity 98
Melting Point 125-135
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,540.00
inventory 5g
10-20 days ฿5,860.00
inventory 25g
10-20 days ฿16,950.00

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Benzaldehyde p-Toluenesulfonylhydrazone
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Benzaldehyde p-toluenesulfonylhydrazone is a key reagent and intermediate in organic synthesis, particularly in the Shapiro reaction for regioselective formation of alkenes via vinyllithium intermediates and in the Bamford-Stevens reaction for generating diazoalkanes and carbenes. It is widely used in the preparation of heterocyclic compounds and other nitrogen-containing structures valuable for pharmaceuticals and agrochemicals. The compound facilitates studies of reaction mechanisms involving carbon-ni

Benzaldehyde p-toluenesulfonylhydrazone is a key reagent and intermediate in organic synthesis, particularly in the Shapiro reaction for regioselective formation of alkenes via vinyllithium intermediates and in the Bamford-Stevens reaction for generating diazoalkanes and carbenes. It is widely used in the preparation of heterocyclic compounds and other nitrogen-containing structures valuable for pharmaceuticals and agrochemicals. The compound facilitates studies of reaction mechanisms involving carbon-nitrogen bond formation/breaking and nitrogen extrusion. In analytical chemistry, it serves as a derivatization agent for detecting and quantifying carbonyl compounds.

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