ETHYL FORMIMIDATE HYDROCHLORIDE

For research use only. Not for therapeutic Use.

  • CAT Number: M076115
  • CAS Number: 16694-46-5
  • Molecular Formula: C3H8ClNO
  • Molecular Weight: 109.553
  • Purity: ≥95%
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<span style="color:#000000;">ETHYL FORMIMIDATE HYDROCHLORIDE (CAS&nbsp;16694-46-5)<span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">&nbsp;<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">is a nitrogen containing organic building block. On heating it undergoes degradation to afford formamidine hydrochloride, ethyl formate and ethyl chloride.</span></span></span></span>


Catalog Number M076115
CAS Number 16694-46-5
Synonyms

Methanimidic acid, ethyl ester, hydrochloride; Ethyl methanimidate hydrochloride

Molecular Formula C3H8ClNO
Purity ≥95%
Storage -20°C
IUPAC Name ethyl methanimidate;hydrochloride
InChI InChI=1S/C3H7NO.ClH/c1-2-5-3-4;/h3-4H,2H2,1H3;1H
InChIKey JPUTTYRVDANTBN-UHFFFAOYSA-N
SMILES CCOC=N.Cl
Reference

<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">1.Rhodd EH and von Richter V. Chemistry of Organic Compounds: Pt. B. Aliphatic compounds , 551-551, (1951)<br />
2.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Cusack, Noel J., Gordon Shaw, and Fatma I. Logemann. &quot;Purines, pyrimidines, and imidazoles part 54. Interconversion of some intermediates in the de novo biosynthesis of purine nucleotides.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of the Chemical Society, Perkin Transactions 1</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;(1980): 2316-2321.</span></span></span></span>

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