| Weight | 121.139 g/mol |
|---|---|
| Formula | C7H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Aminobenzaldehyde (529-23-7)
ortho aminobenzaldehyde
Score:
#54 in Inorganic chemistry
,
#2944 in Biochemistry
,
#7208 in Chemistry
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- Asymmetric synthesis of threonine and partial resolution and retroracemization of .alpha.-amino acids via copper(II) complexes of their Schiff bases with (S)-2-N-(N'-benzylprolyl)aminobenzaldehyde and (S)-2-N-(N'-benzylprolyl)aminoacetophenone. Crystal and molecular structure of a copper(II) complex of glycine Schiff base with (S)-2-N-(N'-benzylprolyl)aminoacetophenone (Journal of the American Chemical Society, 1983)
- One-Pot, Three-Component Synthesis of Dialkyl 1,2-Dihydroquinoline-2,3-Dicarboxylates from Triphenylphosphine, Acetylenic Esters, and Amide Derivatives of 2-Aminobenzaldehyde in Aqueous Acetone (Phosphorus Sulfur and Silicon and The Related Elements, 2005)
- Synthesis of substituted indole from 2-aminobenzaldehyde through [1,2]-aryl shift. (Journal of Organic Chemistry, 2010)
- An Investigation of the Reaction of 2-Aminobenzaldehyde Derivatives with Conjugated Nitro-olefins: An Easy and Efficient Synthesis of 3-Nitro-1,2-dihydroquinolines and 3-Nitroquinolines. (Journal of Organic Chemistry, 2004)
- Cyclization reactions of N-acryloyl-2-aminobenzaldehyde derivatives : formal total synthesis of martinellic acid (Tetrahedron, 2006)
- Studies on novel heterocyclic ring systems. Reaction of 4-hydroxylcoumarin with o-aminobenzaldehyde and 2-mercaptoaniline (Journal of Heterocyclic Chemistry, 1980)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ortho aminobenzaldehyde
-
SMILESC1=CC=C(C(=C1)C=O)N
-
InChIKeyFXWFZIRWWNPPOV-UHFFFAOYSA-N
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