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2-Nitrobenzaldehyde

Short Description:


  • Chemical Name: 2-Nitrobenzaldehyde
  • CAS No.: 552-89-6
  • Deprecated CAS: 2130991-52-3
  • Molecular Formula: C7H5NO3
  • Molecular Weight: 151.122
  • Hs Code.: 29130000
  • European Community (EC) Number: 209-025-3
  • NSC Number: 5713
  • UNII: 48B18Q9B8E
  • DSSTox Substance ID: DTXSID0022060
  • Nikkaji Number: J1.581.631G,J1.615B
  • Wikipedia: 2-Nitrobenzaldehyde
  • Wikidata: Q1055849
  • Metabolomics Workbench ID: 64859
  • ChEMBL ID: CHEMBL166559
  • Mol file: 552-89-6.mol
  • Product Detail

    Product Tags

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    Synonyms:2-nitrobenzaldehyde;o-nitrobenzaldehyde;ortho-nitrobenzaldehyde

    Chemical Property of 2-Nitrobenzaldehyde

    ● Appearance/Colour:Yellow crystalline powder or needles
    ● Vapor Pressure:0.0078mmHg at 25°C
    ● Melting Point:42-44 °C(lit.)
    ● Refractive Index:1.617
    ● Boiling Point:268.2 °C at 760 mmHg
    ● Flash Point:144 °C
    ● PSA:62.89000
    ● Density:1.338 g/cm3
    ● LogP:1.93050

    ● Storage Temp.:Store at RT.
    ● Sensitive.:Air Sensitive
    ● Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly)
    ● Water Solubility.:Insoluble in water.
    ● XLogP3:1.7
    ● Hydrogen Bond Donor Count:0
    ● Hydrogen Bond Acceptor Count:3
    ● Rotatable Bond Count:1
    ● Exact Mass:151.026943022
    ● Heavy Atom Count:11
    ● Complexity:164

    Purity/Quality

    99%min *data from raw suppliers

    2-Nitrobenzaldehyde *data from reagent suppliers

    Safty Information

    ● Pictogram(s):product_img (2)Xn, product (2)Xi
    ● Hazard Codes:Xn,Xi
    ● Statements:22-36/37/38-68
    ● Safety Statements:26-24/25-36/37/39-36

    Useful

    ● Chemical Classes:Nitrogen Compounds -> Other Aromatics (Nitrogen)
    ● Canonical SMILES:C1=CC=C(C(=C1)C=O)[N+](=O)[O-]
    ● Uses2-Nitrobenzaldehyde is a benzaldhyde with a nitro group substituted in the ortho position. 2-Nitrobenzaldehyde is used in the preparation of dyes and colorants such as Indigo carmine. 2-Nitrobenzaldehyde gas been shown to be a useful photoremovable protecting group as well as in the preparation of more effective ones such as o-Nitrophenylethylene glycol.


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