| Weight | 145.161 g/mol |
|---|---|
| Formula | C9H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
isoquinolin-4-ol (3336-49-0)
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- Practical synthesis of 5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-ol (cotarnine) (Journal of Organic Chemistry, 1990)
- Renal vasodilators. The role of the 4-substituent in isoquinolin-3-ol cardiovascular agents: 4-ureido derivatives of isoquinolin-3-ol with selective renal vasodilator properties. (Journal of Medicinal Chemistry, 1989)
- StructureActivity Relationship Studies on Tetrahydroisoquinoline Derivatives: [4-(6,7-Dimethoxy-3,4-dihydro-1H-isoquinolin-2-ylmethyl)biphenyl-4-ol] (MC70) Conjugated through Flexible Alkyl Chains with Furazan Moieties Gives Rise to Potent and Selective Ligands of P-glycoprotein (Journal of Medicinal Chemistry, 2016)
- Substituted 3-isobutyl-9, 10-dimethoxy-1,3,4,6,7,11b-hexahydro-2h-pyrido[2,1-a] isoquinolin-2-ol compounds and methods relating thereto (2007)
- Substituted 3-isobutyl-9,10-dimethoxy-1,3,4,6,7,11b-hexahydro-2-pyrido[2,1-a]isoquinolin-2-ol Compounds and Methods Relating Thereto (2007)
- Composs 3-isobutyl-9, 10-dimthoxy-1,3,4,6,7,11b-hexahydro-2h-pyrido[2,1-a] isoquinolin-2-ol substitus et procds associs (2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C=NC=C2O
-
InChIKeyDXTUTXYCHFWRQC-UHFFFAOYSA-N
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Alternate Names
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Similar Compounds
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isoquinolin-4-ol
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