4-tert-Butylbenzhydrazide

98%

  • Product Code: 118875
  Alias:    p-tert-Butylbenzohydrazide
  CAS:    43100-38-5
Molecular Weight: 192.26 g./mol Molecular Formula: C₁₁H₁₆N₂O
EC Number: 256-090-9 MDL Number: MFCD00014763
Melting Point: 120-127 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
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.
Product Specification:
Test Specification
Melting Point 128-132
Purity (GC) 98-100
Appearance White To Off-White Crystalline Solid
Infrared Spectrometry Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿420.00
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25.000 10-20 days ฿1,690.00
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100.000 10-20 days ฿6,000.00
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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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