| Weight | 171.199 g/mol |
|---|---|
| Formula | C11H9NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
1-Naphthamide (2243-81-4)
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- Synthesis of a potent ()-4-(2-hydroxyphenyl) analogue of the acromelic acids by dearomatising cyclisation of a lithiated N-p-methoxybenzyl-4-methoxy-1-naphthamide (Tetrahedron Letters, 2001)
- Synthesis of atropisomeric 2-(1-aminoalkyl)-1-naphthamides by stereoselective addition of organolithiums to a 2-imino-1-naphthamide (Tetrahedron Letters, 1999)
- N-(.alpha.-hydroxy-2-nitrosobenzyl)-1-naphthamide: a photochemical intermediate (Journal of Organic Chemistry, 1987)
- New N4-substituted piperazine naphthamide derivatives as BACE-1 inhibitors (Journal of Enzyme Inhibition and Medicinal Chemistry, 2009)
- 1-hydroxy-2-naphthamide colored couplers (1947)
- 1-hydroxy-2-naphthamide couplers for color photography (1964)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=CC=C2C(=O)N
-
InChIKeyRMHJJUOPOWPRBP-UHFFFAOYSA-N
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