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[ CAS No. 23772-41-0 ] {[proInfo.proName]}

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Chemical Structure| 23772-41-0
Chemical Structure| 23772-41-0
Structure of 23772-41-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 23772-41-0 ]

CAS No. :23772-41-0 MDL No. :MFCD17392806
Formula : C11H14N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QIRVVAXQAJLVHQ-UHFFFAOYSA-N
M.W : 206.24 Pubchem ID :59441824
Synonyms :

Calculated chemistry of [ 23772-41-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.36
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.34
TPSA : 55.56 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.91
Log Po/w (XLOGP3) : 0.61
Log Po/w (WLOGP) : 0.81
Log Po/w (MLOGP) : 0.85
Log Po/w (SILICOS-IT) : 1.17
Consensus Log Po/w : 1.07

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.67
Solubility : 4.44 mg/ml ; 0.0215 mol/l
Class : Very soluble
Log S (Ali) : -1.35
Solubility : 9.19 mg/ml ; 0.0446 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.4
Solubility : 0.829 mg/ml ; 0.00402 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 23772-41-0 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 23772-41-0 ]

* 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.

  • Upstream synthesis route of [ 23772-41-0 ]
  • Downstream synthetic route of [ 23772-41-0 ]

[ 23772-41-0 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 23772-37-4 ]
  • [ 23772-41-0 ]
YieldReaction ConditionsOperation in experiment
67% With hydrogen In ethanol at 20℃; Intermediate B127: 1-acetyl-5-(methyloxy)-2,3-dihydro-1H-indol-6-amine; A mixture of 1-acetyl-5-(methyloxy)-6-nitro-2,3-dihydro-1 /-/-indole Intermediate B98 (0.56 g, 2.37 mmol) and 10percent Pd on carbon (500 mg) in EtOH (100 ml.) was stirred overnight under 1 atm of H2 gas, then was filtered through a pad of Celite. The filtrate was concentrated to dryness. The residue was dissolved in CH2CI2 and purified by silica gel chromatography using 30-60percent EtOAc/CH2CI2 to obtain 1-acetyl-5- (methyloxy)-2,3-dihydro-1 /-/-indol-6-amine as a white solid (327 mg, 67percent). 1H NMR (400 MHz, DMSO-de) δ ppm 2.09 s, 3H), 2.98 (t, J=8.33 Hz, 2H), 3.70 (s, 3H), 3.99 (t, J=8.33 Hz, 2H), 4.62 (s, 2H), 6.69 (s, 1 H), 7.52 (s, 1 H); ESIMS (M+H)+ = 207.
Reference: [1] Patent: WO2009/20990, 2009, A1, . Location in patent: Page/Page column 151
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