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Diethyl Ethoxymethylenemalonate

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  1. Lutz F. Tietze1,
  2. Holger Geissler1,
  3. C. Wade Downey2

Published Online: 16 SEP 2013

DOI: 10.1002/047084289X.rd194.pub2

e-EROS Encyclopedia of Reagents for Organic Synthesis

e-EROS Encyclopedia of Reagents for Organic Synthesis

COMPOUND RECORD : 1H-Pyrazol-3-amine


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Summary

Compound Information

FormulaC3H5N3
Molecular Weight83.0919
SynonymsNot available

Structure Descriptors

SMILES:NC1=CC=NN1
InChI:1S/C3H5N3/c4-3-1-2-5-6-3/h1-2H,(H3,4,5,6)
InChIKey:JVVRJMXHNUAPHW-UHFFFAOYSA-N

Other articles that contain this structure:

  1. Synthesis of 2,4-dimethylpyrazolo[1,5-a]-1,3,5-triazine

    Journal of Heterocyclic Chemistry

    Volume 10, Issue 5, October 1973, Page: 885, Anthony H. Albert, Roland K. Robins and Darrell E. O'Brien

    Version of Record online : 11 MAR 2009, DOI: 10.1002/jhet.5570100539

  2. 3(5)-Aminopyrazole

    Organic Syntheses

    H. Dorn and A. Zubek

    Published Online : 28 APR 2003, DOI: 10.1002/0471264180.os048.03

  3. Nucleosides CV. Synthesis of the 8-((β-D-ribofuranosyl)pyrazolo[1,5-a]-1,3,5-triazine isosteres of adenosine and inosine

    Journal of Heterocyclic Chemistry

    Volume 13, Issue 6, December 1976, Pages: 1305–1308, S. Y-K. Tam, J-S. Hwang, F. G. De Las Heras, R. S. Klein and J. J. Fox

    Version of Record online : 2 APR 2009, DOI: 10.1002/jhet.5570130631

  4. Basicity of azoles. VII. Basicity of C-aminopyrazoles in relation to tautomeric and protonation studies

    Journal of Heterocyclic Chemistry

    Volume 22, Issue 4, July 1985, Pages: 997–1000, Javier Catalán, Margarita Menéndez, José Laynez, Rosa María Claramunt, Marta Bruix, Javier De Mendoza and José Elguero

    Version of Record online : 6 APR 2009, DOI: 10.1002/jhet.5570220413

  5. Synthesis of 6-quinoxalinyldihydropyrazolo[1,5-a]pyrimidin-7-ones by a ring transformation. Tautomeric structure of dihydropyrazolo[1,5-a]pyrimidin-7-ones in a solution

    Journal of Heterocyclic Chemistry

    Volume 27, Issue 7, November 1990, Pages: 2203–2205, Yoshihisa Kurasawa, Ho Sik Kim, Atsushi Takada and Yoshihisa Okamoto

    Version of Record online : 11 MAR 2009, DOI: 10.1002/jhet.5570270761

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