Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Synthesis and Structure of 2,6-Dihalo-Benzenone-Indophenylacetate and Benzenone-lndo-3′,5′-Dihalo-Phenylacetate

Abstract

HITHERTO only one compound has been isolated after the esterification of dihalo-benzenone-indo-phenol with acetic anhydride; this compound was assumed to be 2,6-dihalo-benzenone-indophenylacetate1:

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Kramer, D. N., and Gamson, R. M., Anal. Chem., 30, 251 (1958).

    Article  CAS  Google Scholar 

  2. Heller, G., Chem. Ann., 392, 16 (1912).

    Article  Google Scholar 

  3. Weisberger, A., “Tech. of Org. Chem.”, 9, “Chem. Applications of Spectroscopy” (Interscience Pub., New York, 1956).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

DE BORST, C., HOOGE, F. & ARKENBOUT, G. Synthesis and Structure of 2,6-Dihalo-Benzenone-Indophenylacetate and Benzenone-lndo-3′,5′-Dihalo-Phenylacetate. Nature 182, 1017–1018 (1958). https://doi.org/10.1038/1821017a0

Download citation

  • Issue date:

  • DOI: https://doi.org/10.1038/1821017a0

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing