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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

Term:4-nitrobenzaldehyde
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Accession:CHEBI:66926 term browser browse the term
Definition:A C-nitro compound that is benzaldehyde substituted at the para-position with a nitro group.
Synonyms:related_synonym: Formula=C7H5NO3;   InChI=1S/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H;   InChIKey=BXRFQSNOROATLV-UHFFFAOYSA-N;   SMILES=[O-][N+](=O)c1ccc(C=O)cc1;   p-nitrobenzaldehyde
 xref: CAS:555-16-8
 xref_mesh: MESH:C029915
 xref: MetaCyc:CPD-703;   PMID:1650428;   PMID:19066862;   PMID:19360727;   PMID:22318956;   PMID:22803669;   Reaxys:386796;   Wikipedia:4-Nitrobenzaldehyde


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      group 0
        inorganic group 0
          nitro group 0
            nitro compound 0
              C-nitro compound 0
                4-nitrobenzaldehyde 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            formyl group 0
                                              aldehyde 0
                                                arenecarbaldehyde 0
                                                  benzaldehydes 0
                                                    4-nitrobenzaldehyde 0
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