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[ CAS No. 50593-30-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 50593-30-1
Chemical Structure| 50593-30-1
Structure of 50593-30-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 50593-30-1 ]

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Product Details of [ 50593-30-1 ]

CAS No. :50593-30-1 MDL No. :MFCD00464866
Formula : C8H9N3 Boiling Point : -
Linear Structure Formula :- InChI Key :MHCWLERQNFATHZ-UHFFFAOYSA-N
M.W : 147.18 Pubchem ID :590220
Synonyms :

Calculated chemistry of [ 50593-30-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.12
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 45.4
TPSA : 43.84 ?2

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) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.3
Log Po/w (XLOGP3) : 1.25
Log Po/w (WLOGP) : 1.16
Log Po/w (MLOGP) : 0.84
Log Po/w (SILICOS-IT) : 0.71
Consensus Log Po/w : 1.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.15
Solubility : 1.05 mg/ml ; 0.00715 mol/l
Class : Soluble
Log S (Ali) : -1.77
Solubility : 2.51 mg/ml ; 0.017 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.09
Solubility : 1.19 mg/ml ; 0.00807 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.48

Safety of [ 50593-30-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 50593-30-1 ]

* 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 [ 50593-30-1 ]

[ 50593-30-1 ] Synthesis Path-Downstream   1~11

  • 1
  • [ 50593-30-1 ]
  • [ 1147550-11-5 ]
  • 2-methyl-5-thiocyanato-2<i>H</i>-indazol-6-ylamine [ No CAS ]
  • 2
  • [ 6850-22-2 ]
  • [ 50593-30-1 ]
YieldReaction ConditionsOperation in experiment
89.5% With palladium 10% on activated carbon; hydrogen; In ethanol; at 20℃; for 12.0h; General procedure: 10% Palladium carbon (water content 51.7%, 1 g) was added to a solution of 2a (7.50 g, 40 mmol) in ethanol (150 ml), and the mixture was stirred under hydrogen atmosphere at room temperature for 12 h. The catalyst was removed by filtration and washed with ethanol. The filtrate and washings were combined and the solvent was distilled off under reduced pressure to give 3a as alight beige solid (6.05, 95.0% yield).
  • 5
  • [ 50593-30-1 ]
  • [ 16463-38-0 ]
  • [ 132283-43-3 ]
  • 8
  • [ 50593-30-1 ]
  • [ 28899-97-0 ]
  • 2-methyl-6-phenylamino-1H-indazole [ No CAS ]
  • 9
  • [ 50-00-0 ]
  • [ 50593-30-1 ]
  • C19H18N6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With iron; ammonium chloride; In ethanol; water;Reflux; General procedure: [000414j The title compound has been synthesized by following the general procedure described above for reduction using the nitro compound 2 and Fe/NH4C1.
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