4-tert-Butylbenzhydrazide

98%

Reagent Code: #118875
label
Alias p-tert-Butylbenzohydrazide
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CAS Number 43100-38-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.26 g/mol
Formula C₁₁H₁₆N₂O
badge Registry Numbers
EC Number 256-090-9
MDL Number MFCD00014763
thermostat Physical Properties
Melting Point 120-127 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

4-tert-Butylbenzhydrazide is primarily used in organic synthesis as a key intermediate for the preparation of various hydrazone derivatives. These derivatives are often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory, antimicrobial, and antitumor properties. Additionally, it serves as a building block in the creation of agrochemicals, where it contributes to the formulation of pesticides and herbicides. The compound is also utilized in research laboratories for studying reaction mechanisms and developing novel chemical entities with specific biological activities. Its role in the synthesis of Schiff bases further extends its application in material science, particularly in the design of coordination polymers and metal-organic frameworks.

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Test Parameter Specification
Melting Point 128-132
Purity (GC) 98-100
Appearance White To Off-White Crystalline Solid
Infrared Spectrometry Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿6,000.00
inventory 25g
10-20 days ฿1,690.00
inventory 5g
10-20 days ฿420.00
4-tert-Butylbenzhydrazide
4-tert-Butylbenzhydrazide is primarily used in organic synthesis as a key intermediate for the preparation of various hydrazone derivatives. These derivatives are often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory, antimicrobial, and antitumor properties. Additionally, it serves as a building block in the creation of agrochemicals, where it contributes to the formulation of pesticides and herbicides. The compound is also utilized in research laboratories for studying reaction mechanisms and developing novel chemical entities with specific biological activities. Its role in the synthesis of Schiff bases further extends its application in material science, particularly in the design of coordination polymers and metal-organic frameworks.
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