| Weight | 162.188 g/mol |
|---|---|
| Formula | C10H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
5-Methoxy-1-indanone (5111-70-6)
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- Efficient catalytic asymmetric alkylations. 3. A kinetic and mechanistic study of the enantioselective phase-transfer methylation of 6,7-dichloro-5-methoxy-2-phenyl-1-indanone (Journal of Organic Chemistry, 1987)
- Selective inhibition of the chymotrypsin-like activity of the 20S proteasome by 5-methoxy-1-indanone dipeptide benzamides (Bioorganic & Medicinal Chemistry Letters, 1998)
- Optical purity determination and 1H-NMR spectral simplification with lanthanide shift reagents. VIII: An indacrinone precursor, 6,7-dichloro-5-methoxy-2-methyl-2-phenyl-1-indanone (Journal of Pharmaceutical and Biomedical Analysis, 1986)
- Crystal Structure of 2-(1-Hydroxycyclopropyl)-2, 5-dimethyl-6-methoxy-1-indanone (Analytical Sciences, 1997)
- ChemInform Abstract: SYNTHESIS OF 3,3-DIMETHYL-5-METHOXY-1-INDANONE AND 9,9-DIMETHYL-2-METHOXY-5-BENZOSUBERONE (ChemInform, 1982)
- ChemInform Abstract: Efficient Catalytic Asymmetric Alkylations. Part 3. A Kinetic and Mechanistic Study of the Enantioselective Phase-Transfer Methylation of 6,7-Dichloro-5-methoxy-2-phenyl-1-indanone. (ChemInform, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC2=C(C=C1)C(=O)CC2
-
InChIKeyQOPRWBRNMPANKN-UHFFFAOYSA-N
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