52094-94-7

Basic information

• Product Name: 2-(2-CHLOROPHENOXY)PROPANOHYDRAZIDE
• Synonyms: 2-(2-CHLOROPHENOXY)PROPANOHYDRAZIDE;2-(2-chlorophenoxy)propanohydrazide(SALTDATA: FREE);2-(2-chlorophenoxy)propanehydrazide;2-(2-chlorophenoxy)propionohydrazide
• CAS NO: 52094-94-7
• Molecular Formula: C₉H₁₁ClN₂O₂
• Molecular Weight: 214.65
• Mol File: 52094-94-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 415.2°C at 760 mmHg
• Flash Point: 204.9°C
• Appearance: /
• Density: 1.274g/cm³
• Vapor Pressure: 4.19E-07mmHg at 25°C
• Refractive Index: 1.557
• CAS DataBase Reference: 2-(2-CHLOROPHENOXY)PROPANOHYDRAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-CHLOROPHENOXY)PROPANOHYDRAZIDE(52094-94-7)
• EPA Substance Registry System: 2-(2-CHLOROPHENOXY)PROPANOHYDRAZIDE(52094-94-7)

Safety Data

• Hazardous Substances Data: 52094-94-7(Hazardous Substances Data)

Usage

Chemical classification

propanohydrazide

Contains a chlorophenoxy group

derivative of phenol

Contains a propanohydrazide group

derivative of hydrazine and propanoic acid

Industrial applications

potential use as a pesticide or herbicide

Handling precautions

may have potential health and environmental risks if not properly managed.

InChI:InChI=1/C9H11ClN2O2/c1-6(9(13)12-11)14-8-5-3-2-4-7(8)10/h2-6H,11H2,1H3,(H,12,13)

Upstream product

• 52094-99-2 Ethyl 2-(2-chlorophenoxy)propionate 

Downstream Products

• 83797-81-3 5-[1-(2-Chloro-phenoxy)-ethyl]-3H-[1,3,4]oxadiazole-2-thione 
• 97841-49-1 C₄₆H₃₈Cl₂N₆O₄S₂ 
• 97841-39-9 C₃₈H₃₆Cl₂N₆O₄S₂ 
• 97841-38-8 C₂₆H₂₈Cl₂N₆O₄S₂ 

Relevant articles and documents

Synthesis and Insecticidal Evaluation of Novel N-pyridylpyrazole Derivatives Containing Diacylhydrazine/1,3,4-Oxadiazole Moieties

Two series of novel N-pyridylpyrazole derivatives containing diacylhydrazine/1,3,4-oxadiazole moieties were designed and synthesized based on the structure of chlorantraniliprole and characterized via 1H-NMR, 13C-NMR, IR, MS, and elemental analysis. The preliminary bioassay indicated that some of the title compounds I and II exhibited larvicidal activities against Mythimna separata with 90–100% death rates at 500?mg/L. The further test showed that these compounds had weak insecticidal activity against Mythimna separata and Plutella xylostella at 200?mg/L and might be not suitable as insecticide lead compound for further optimization.