| Weight | 171.243 g/mol |
|---|---|
| Formula | C12H13N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
2,3,4,9-Tetrahydro-1H-carbazole (942-01-8)
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- Design and synthesis of 2,3,4,9-tetrahydro-1H-carbazole and 1,2,3,4-tetrahydro-cyclopenta[b]indole derivatives as non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA polymerase. (Bioorganic & Medicinal Chemistry Letters, 2006)
- Synthesis of 9-substituted 2,3,4,9-tetrahydro-1H-carbazole derivatives and evaluation of their anti-prion activity in TSE-infected cells. (European Journal of Medicinal Chemistry, 2011)
- Potent and highly selective DP1 antagonists with 2,3,4,9-tetrahydro-1H-carbazole as pharmacophore (Bioorganic & Medicinal Chemistry Letters, 2010)
- Discovery of 6-Fluoro-5-(R)-(3-(S)-(8-fluoro-1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)-2-methylphenyl)-2-(S)-(2-hydroxypropan-2-yl)-2,3,4,9-tetrahydro-1H-carbazole-8-carboxamide (BMS-986142): A Reversible Inhibitor of Brutons Tyrosine Kinase (BTK) Conformationally Constrained by Two Locked Atropisomers (Journal of Medicinal Chemistry, 2016)
- Synthesis of 2,3-dihydronaphtho[2,3-d][1,3]thiazole-4,9-diones and 2,3-dihydroanthra[2,3-d][1,3]thiazole-4,11-diones and novel ring contraction and fusion reaction of 3H-spiro[1,3-thiazole-2,1'-cyclohexanes] into 2,3,4,5-tetrahydro-1H-carbazole-6,11-diones (Beilstein Journal of Organic Chemistry, 2013)
- Methyl 9-methyl-1-oxo-2,3,4,9-tetrahydro-1H-carbazole-2-carboxylate (Acta Crystallographica Section E: Crystallographic Communications, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCC2=C(C1)C3=CC=CC=C3N2
-
InChIKeyXKLNOVWDVMWTOB-UHFFFAOYSA-N
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