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CAS No. : | 1081-05-6 | MDL No. : | MFCD06659780 |
Formula : | C10H9ClN2O2 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | - |
M.W : | 224.64 g/mol | Pubchem ID : | - |
Synonyms : |
|
Num. heavy atoms : | 15 |
Num. arom. heavy atoms : | 9 |
Fraction Csp3 : | 0.2 |
Num. rotatable bonds : | 3 |
Num. H-bond acceptors : | 3.0 |
Num. H-bond donors : | 1.0 |
Molar Refractivity : | 57.19 |
TPSA : | 54.98 Ų |
GI absorption : | High |
BBB permeant : | Yes |
P-gp substrate : | No |
CYP1A2 inhibitor : | Yes |
CYP2C19 inhibitor : | No |
CYP2C9 inhibitor : | No |
CYP2D6 inhibitor : | No |
CYP3A4 inhibitor : | No |
Log Kp (skin permeation) : | -5.73 cm/s |
Log Po/w (iLOGP) : | 1.91 |
Log Po/w (XLOGP3) : | 2.73 |
Log Po/w (WLOGP) : | 2.39 |
Log Po/w (MLOGP) : | 1.9 |
Log Po/w (SILICOS-IT) : | 2.81 |
Consensus Log Po/w : | 2.35 |
Lipinski : | 0.0 |
Ghose : | None |
Veber : | 0.0 |
Egan : | 0.0 |
Muegge : | 0.0 |
Bioavailability Score : | 0.55 |
Log S (ESOL) : | -3.2 |
Solubility : | 0.142 mg/ml ; 0.000633 mol/l |
Class : | Soluble |
Log S (Ali) : | -3.54 |
Solubility : | 0.065 mg/ml ; 0.000289 mol/l |
Class : | Soluble |
Log S (SILICOS-IT) : | -4.02 |
Solubility : | 0.0217 mg/ml ; 0.0000964 mol/l |
Class : | Moderately soluble |
PAINS : | 0.0 alert |
Brenk : | 0.0 alert |
Leadlikeness : | 1.0 |
Synthetic accessibility : | 1.95 |
Signal Word: | Warning | Class: | |
Precautionary Statements: | P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313 | UN#: | |
Hazard Statements: | H315-H319 | Packing Group: | |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With pyridine Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
5-Chlor-3-carboxy-indazol, konz. H2SO4 in sd. EtOH (3h); |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1.1: sodium hydroxide / water / 0.5 h / 50 °C 1.2: 1 h / 0 °C 1.3: 18 h / 0 - 20 °C 2.1: sulfuric acid / 5 h / 100 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
27% | With triethylamine In dichloromethane at 0 - 20℃; for 4h; |
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