2-Aminobenzaldehyde

2-Aminobenzaldehyde.svg 132 2-Aminobenzaldehyde ortho-Aminobenzaldehyde2-Formylaniline2-Aminobenzenecarbaldehyde 529-23-7 correct CAS correct FDA EG769PG2AX 68255 208-454-3 61553 1S/C7H7NO/c8-7-4-2-1-3-6(7)5-9/h1-5H,8H2 FXWFZIRWWNPPOV-UHFFFAOYSA-N C1=CC=C(C(=C1)C=O)N 7 7 1 1 yellow solid 32-34 good 2-Aminobenzaldehyde is an organic compound with the formula C6H4(NH2)CHO. It is one of three isomers of aminobenzaldehyde. It is a low-melting yellow solid that is soluble in water.10.1002/047084289X.ra088 2-Aminobenzaldehyde Encyclopedia of Reagents for Organic Synthesis 2001 Thummel Randolph P. 0471936235 Preparation and reactions It is usually prepared by reduction of 2-nitrobenzaldehyde with ironOrg. Synth. 2012 89 274 10.15227/orgsyn.089.0274 o-Aminobenzaldehyde, Redox-Neutral Aminal Formation and Synthesis of Deoxyvasicinone Chen Zhang Chandra Kanta De Daniel Seidel free or iron(II) sulfate.Org. Synth. 1948 28 11 10.15227/orgsyn.028.0011 free o-Aminobenzaldehyde Lee Irvin Smith J. W. Opie Like related aminoaldehydes, it is unstable with respect to self-condensation. 2-Aminobenzaldehyde is used to prepare quinolines by the Friedländer synthesis: center|450px|The Friedländer synthesis By template reactions, it also forms trimeric and tetrameric condensation products that have been studied as ligands. thumb|left|154px|Structure of nickel-aquo nitrate complex of the ligand derived from condensation of three equivalents of 2-aminobenzaldehyde.Fleischer E. B. Klem E. 1965 The Structure of a Self-Condensation Product of o-Aminobenzaldehyde in the Presence of Nickel Ions Inorganic Chemistry 4 5 637–642 10.1021/ic50027a008 References Category:Benzaldehydes Category:2-Aminophenyl compounds