Weight | 131.134 g/mol |
---|---|
Formula | C8H5NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-Cyanobenzaldehyde (24964-64-5)
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- SYNTHESIS OF 1,3-DIIMINOISOINDOLINES FROM 2-CYANOBENZALDEHYDE. REACTION OF N-(2-CYANOBENZYLIDENE)ANILINES WITH ELEMENTAL SULFUR IN LIQUID AMMONIA AND AMINES (Chemistry Letters, 1985)
- NOVEL SYNTHESIS OF 3-(N-SUBSTITUTED AMINO)-1-ISOINDOLENONES FROM 2-CYANOBENZALDEHYDE WITH AMINES (Chemistry Letters, 1984)
- Novel One-Pot Synthesis of 2-Substituted 3-Alkoxyisoindolin-1-imine Derivatives from 2-Cyanobenzaldehyde, Amine, and Alcohol (Synthesis, 2012)
- Platinum(II)-Promoted [2+3] Cycloaddition of Azide with 4-Cyanobenzaldehyde, a Schiff Base Derivative or Dicyanobenzenes To Give Formyl-, Amino(imino)- or Cyano-Functionalized Tetrazolato Complexes (European Journal of Inorganic Chemistry, 2009)
- The conformational distribution of 2-cyanobenzaldehyde and 3-cyanobenzaldehyde in solution and in the vapor (Canadian Journal of Chemistry, 1991)
- Synthesis and Reactions of 3-Substituted Isoindolenones from o-Cyanobenzaldehyde (Heterocycles, 1986)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)C=O)C#N
-
InChIKeyHGZJJKZPPMFIBU-UHFFFAOYSA-N
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