6293-87-4

Basic information

• Product Name: 2-Nitrophenylhydrazine hydrochloride
• Synonyms: (o-nitrophenyl)-hydrazinhydrochloride;2-NITROPHENYLHYDRAZINE HYDROCHLORIDE;2-NitrophenylhydrazineHCl;2-Nitrophenylhydrazin;2-Hydrazinonitrobenzene hydrochloride;2-nitrophenylhydrazine hydrochloride, 98%, derivatization grade;2-Nitrophenylhydrazine hydrochloride, derivatization grade;The 2- nitrophenyl hydrazine hydrochloride
• CAS NO: 6293-87-4
• Molecular Formula: C₆H₇N₃O₂*ClH
• Molecular Weight: 189.6
• Product Categories: Phenylhydrazine
• Mol File: 6293-87-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 314.3 °C at 760 mmHg
• Flash Point: 143.9 °C
• Appearance: /
• Vapor Pressure: 0.000469mmHg at 25°C
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 2-Nitrophenylhydrazine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nitrophenylhydrazine hydrochloride(6293-87-4)
• EPA Substance Registry System: 2-Nitrophenylhydrazine hydrochloride(6293-87-4)

Safety Data

• Statements: 20-21-36-37-22
• Safety Statements: 26-36/37/39-44-28
• RIDADR: 1325
• RTECS: MV8230000
• HazardClass: 4.1
• PackingGroup: II
• Hazardous Substances Data: 6293-87-4(Hazardous Substances Data)

Usage

Chemical Properties

Yellow to orange powder

InChI:InChI=1/C6H7N3O2.ClH/c7-8-5-3-1-2-4-6(5)9(10)11;/h1-4,8H,7H2;1H

Upstream product

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Downstream Products

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• 100033-06-5 Malonsaeureethylester-2-nitro-phenylhydrazidin-Hydrochlorid 
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Relevant articles and documents

Design, synthesis, crystal structures, and insecticidal activities of eight-membered azabridge neonicotinoid analogues

Three series of novel azabridge neonicotinoid analogues were designed and synthesized, which were constructed by starting material A, glutaraldehyde, and primary amine hydrochlorides (aliphatic amines, phenylhydrazines, and anilines). Most of the eight-membered azabridge compounds presented higher insecticidal activities than oxabridged compound B against cowpea aphid (Aphis craccivora) and brown planthopper (Nilaparvata lugens). Compared with imidacloprid, some azabridged compounds exhibited excellent insecticidal activity against brown planthopper. The crystal structures and bioassay indicated that changing bridge atoms from O to N could lead to entirely different conformations, which might be the important influential factor of the bioactivities.