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[ CAS No. 1081-05-6 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 1081-05-6
Chemical Structure| 1081-05-6
Chemical Structure| 1081-05-6
Structure of 1081-05-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1081-05-6 ]

CAS No. :1081-05-6 MDL No. :MFCD06659780
Formula : C10H9ClN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :RYZAFUIELFHCSW-UHFFFAOYSA-N
M.W : 224.64 Pubchem ID :12689363
Synonyms :

Calculated chemistry of [ 1081-05-6 ]

Physicochemical Properties

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

Pharmacokinetics

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

Lipophilicity

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

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.55

Water Solubility

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

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.95

Safety of [ 1081-05-6 ]

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:

Application In Synthesis of [ 1081-05-6 ]

* 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.

  • Downstream synthetic route of [ 1081-05-6 ]

[ 1081-05-6 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 10400-19-8 ]
  • [ 1081-05-6 ]
  • 5-Chloro-1-(pyridine-3-carbonyl)-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 2
  • [ 3282-30-2 ]
  • [ 1081-05-6 ]
  • 5-Chloro-1-(2,2-dimethyl-propionyl)-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 4
  • [ 98-88-4 ]
  • [ 1081-05-6 ]
  • 1-Benzoyl-5-chloro-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 5
  • [ 122-01-0 ]
  • [ 1081-05-6 ]
  • chloro-5 N1-chlorobenzoyl 1H-carboxylate d'ethyle-3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 6
  • [ 38835-18-6 ]
  • [ 1081-05-6 ]
  • 5-Chloro-1-[2-(6-methoxy-naphthalen-2-yl)-propionyl]-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 7
  • [ 1081-05-6 ]
  • [ 75-36-5 ]
  • 1-Acetyl-5-chloro-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
  • 8
  • [ 1081-05-6 ]
  • [ 21615-34-9 ]
  • 5-Chloro-1-(2-methoxy-benzoyl)-1H-indazole-3-carboxylic acid ethyl ester [ No CAS ]
YieldReaction ConditionsOperation in experiment
With pyridine Heating;
YieldReaction ConditionsOperation in experiment
5-Chlor-3-carboxy-indazol, konz. H2SO4 in sd. EtOH (3h);
  • 10
  • [ 64-17-5 ]
  • [ 1077-95-8 ]
  • [ 1081-05-6 ]
  • 11
  • [ 17630-76-1 ]
  • [ 1081-05-6 ]
YieldReaction ConditionsOperation 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
  • 12
  • [ 1081-05-6 ]
  • [ 1711-06-4 ]
  • [ 1448314-59-7 ]
YieldReaction ConditionsOperation in experiment
27% With triethylamine In dichloromethane at 0 - 20℃; for 4h;
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