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[ CAS No. 10553-08-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 10553-08-9
Chemical Structure| 10553-08-9
Structure of 10553-08-9 * Storage: {[proInfo.prStorage]}
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Quality Control of [ 10553-08-9 ]

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Product Details of [ 10553-08-9 ]

CAS No. :10553-08-9 MDL No. :MFCD22556380
Formula : C9H8N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :BGLMRHYPBSQOTA-UHFFFAOYSA-N
M.W : 176.17 Pubchem ID :15453466
Synonyms :

Calculated chemistry of [ 10553-08-9 ]

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.11
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 52.09
TPSA : 61.61 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) : -5.78 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.49
Log Po/w (XLOGP3) : 2.24
Log Po/w (WLOGP) : 2.38
Log Po/w (MLOGP) : 1.51
Log Po/w (SILICOS-IT) : 0.77
Consensus Log Po/w : 1.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.79
Solubility : 0.286 mg/ml ; 0.00162 mol/l
Class : Soluble
Log S (Ali) : -3.17
Solubility : 0.119 mg/ml ; 0.000677 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.05
Solubility : 0.157 mg/ml ; 0.000893 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.79

Safety of [ 10553-08-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 10553-08-9 ]

* 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 [ 10553-08-9 ]

[ 10553-08-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 87240-06-0 ]
  • [ 594-27-4 ]
  • [ 10553-08-9 ]
YieldReaction ConditionsOperation in experiment
0.35 g (2.0 mmol, 74%) In N,N-dimethyl-formamide 4 7-Methyl-5-nitroindole 7-Methyl-5-nitroindole To a solution of 7-bromo-5-nitroindoline (0.65 g, 2.7 mmol) in 10 mL of DMF were added tetramethyltin (1.0 mL, 7.3 mmol) and bis(triphenylphosphine)palladium(II) chloride (0.10 g) in a portion and resulting mixture was stirred in sealed tube for 12 h at 140° C. The reaction mixture was concentrated in vacuo, providing a dark oily residue which was subjected to column chromatography (CHCl3, neat) to yield 0.35 g (2.0 mmol, 74%) of the desired product.
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