Abstract
Thiele and Dralle1 reported the condensation of aminoguanidine nitrate and α-nitroso-β-naphthol with the formation of α-oximino-β-naphthylidene-aminoguanidine nitrate. They observed that the initial reaction product (A) underwent further change to a material of formula C11H8N4O (B) on treatment with boiling water, with loss of ammonium nitrate. They gave no structure for (B).
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 51 print issues and online access
$199.00 per year
only $3.90 per issue
Buy this article
- Purchase on Springer Link
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Similar content being viewed by others
References
Thiele and Dralle, Ann., 302, 275 (1898).
Lang, Z. physiol. Chem., 208, 273 (1932).
Curatolo, Gazz. chim. ital., 20, 585 (1890). Sakaguchi, J. Biochem. Japan, 5, 25 (1925).
Vogel, “Practical Organic Chemistry”, 620 (1948). Van Slyke, J. Biol. Chem., 12, 275 (1912). Mulliken, “Identification of Organic Compounds”, 2, 34 (1916). Willgerodt, Ber., 9, 977 (1876).
Vide Verley and Bölsing, Ber., 34, 3354 (1901).
Ponzio, Gazz. chim. ital., 28, (i), 173 (1898).
De, Quart. J. Ind. Chem. Soc., 4, 183 (1927). De and Dutt, ibid., 7, 537 (1930).
Carroll, thesis, Univ. Coll., Cork (1949).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
SCOTT, F., REILLY, J. Oxy-Triazines from Aminoguanidine. Nature 169, 584–585 (1952). https://doi.org/10.1038/169584a0
Issue Date:
DOI: https://doi.org/10.1038/169584a0
Comments
By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.