22179-77-7

Basic information

• Product Name: 3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE
• Synonyms: 3-CHLOROBENZAMIDE OXIME;3-CHLORO-N-HYDROXY-BENZAMIDINE;3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE;BUTTPARK 99\12-100;3-Chloro-N'-hydroxybenzenecarboximideamide;3-Chloro-N'-hydroxybenzenecarboximidamide 97%;3-Chlorobenzamidoxime;3-Chlorobenzamidoxime 97%
• CAS NO: 22179-77-7
• Molecular Formula: C₇H₇ClN₂O
• Molecular Weight: 170.6
• Mol File: 22179-77-7.mol
• Article Data: 31

Chemical Properties

• Melting Point: 115 °C
• Boiling Point: 350.4 °C at 760 mmHg
• Flash Point: 165.7 °C
• Appearance: /
• Density: 1.36 g/cm³
• Vapor Pressure: 1.64E-05mmHg at 25°C
• Refractive Index: 1.6
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE(22179-77-7)
• EPA Substance Registry System: 3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE(22179-77-7)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38-44
• Safety Statements: 22-26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 22179-77-7(Hazardous Substances Data)

Usage

General Description

3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE is a chemical compound with the molecular formula C7H6ClN3O2. It is a derivative of benzene carboximidamide and contains a hydroxyl group and a chlorine atom attached to the benzene ring. This chemical is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also known to exhibit antimicrobial and antiviral properties, making it potentially useful in the development of medical treatments. However, given its reactive nature and potential hazards, proper handling and storage procedures are necessary when working with 3-CHLORO-N'-HYDROXYBENZENECARBOXIMIDAMIDE.

InChI:InChI=1/C7H7ClN2O/c8-6-3-1-2-5(4-6)7(9)10-11/h1-4,11H,(H2,9,10)

Upstream product

• 587-04-2 m-Chlorobenzaldehyde 
• 766-84-7 3-chloro-benzonitrile 
• 67-56-1 methanol 

Downstream Products

• 93048-81-8 3-chloro-N-chloroacetoxy-benzamidine 
• 1403775-94-9 C₁₆H₁₈ClN₃O₃ 
• 1351647-27-2 C₁₁H₁₀ClN₃O*ClH 
• 1403776-23-7 C₁₉H₁₉ClF₃N₃O₂ 
• 1403776-22-6 C₁₉H₂₂ClN₃O₂ 
• 1403776-21-5 C₁₉H₂₂ClN₃O₂ 
• 1403776-20-4 C₁₈H₁₈ClF₂N₃O₂ 
• 1403776-19-1 C₁₆H₁₆ClN₃O₃ 
• 1403776-18-0 C₁₆H₁₆ClN₃O₂ 
• 1403776-17-9 C₁₈H₂₀ClN₃O₂ 
• 1403775-85-8 C₁₈H₁₃ClFN₃O₂ 
• 1403775-84-7 C₁₈H₁₃ClFN₃O₂ 

Relevant articles and documents

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A highly efficient rhodium(III)-catalyzed synthesis of novel functionalized indene derivatives has been achieved via C?H activation/intramolecular aldol condensation. This cascade reaction is an atom economical protocol which could be further applied to build more complex compounds. (Figure presented.).

Pharmacophore requirements for HIV-1 reverse transcriptase inhibitors that selectively “Freeze” the pre-translocated complex during the polymerization catalytic cycle

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