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[ CAS No. 129075-49-6 ] {[proInfo.proName]}

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Chemical Structure| 129075-49-6
Chemical Structure| 129075-49-6
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Quality Control of [ 129075-49-6 ]

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Product Details of [ 129075-49-6 ]

CAS No. :129075-49-6 MDL No. :MFCD07196047
Formula : C10H11NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OESOLVOZJGIVMY-UHFFFAOYSA-N
M.W : 177.20 Pubchem ID :7385098
Synonyms :

Calculated chemistry of [ 129075-49-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 52.7
TPSA : 38.33 ?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) : -6.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.84
Log Po/w (XLOGP3) : 1.2
Log Po/w (WLOGP) : 0.6
Log Po/w (MLOGP) : 1.14
Log Po/w (SILICOS-IT) : 2.07
Consensus Log Po/w : 1.37

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.97
Solubility : 1.9 mg/ml ; 0.0107 mol/l
Class : Very soluble
Log S (Ali) : -1.6
Solubility : 4.44 mg/ml ; 0.025 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.29
Solubility : 0.0903 mg/ml ; 0.000509 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.63

Safety of [ 129075-49-6 ]

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

Application In Synthesis of [ 129075-49-6 ]

* 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 [ 129075-49-6 ]

[ 129075-49-6 ] Synthesis Path-Downstream   1~12

  • 1
  • [ 85834-35-1 ]
  • [ 129075-49-6 ]
  • 2-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-ethyl}-5-methoxy-3,4-dihydro-2<i>H</i>-isoquinolin-1-one [ No CAS ]
  • 3
  • [ 56469-02-4 ]
  • [ 333-27-7 ]
  • [ 129075-49-6 ]
  • 4
  • [ 103205-24-9 ]
  • [ 129075-49-6 ]
  • 5
  • C11H13NO4S [ No CAS ]
  • [ 30557-06-3 ]
  • [ 129075-49-6 ]
  • 6
  • 4-methoxy-indan-1-one oxime [ No CAS ]
  • [ 129075-49-6 ]
  • 8
  • [ 56469-02-4 ]
  • [ 129075-49-6 ]
YieldReaction ConditionsOperation in experiment
5.3 g (89%) With dimethyl sulfate; In methanol; sodium hydroxide; water; EXAMPLE V 3,4-Dihydro-5-methoxy-1(2H)-isoquinolinone To a refluxing solution of 5.5 g (33.7 mmol) of 3,4-dihydro-5-hydroxy-1(2H)-isoquinolinone in 35 ml of 2N NaOH and 70 ml of methanol was added 4 ml of dimethyl sulfate. At two-hour intervals additional amounts of NaOH and dimethyl sulfate were added and the reaction was heated under reflux conditions overnight. The mixture was concentrated, diluted with 300 ml of water, and acidified (pH 2-3) with concentrated sulfuric acid. The solid which formed was collected and dried to give 5.3 g (89%) of material sufficiently pure for the next step. An analytical sample was obtained by recrystallization from acetone; mp 147-149.
  • 9
  • [ 56469-02-4 ]
  • [ 74-88-4 ]
  • [ 129075-49-6 ]
YieldReaction ConditionsOperation in experiment
Intermediate Q5-Methoxy-3,4-dihydro-2H-isoquinolin-1 -oneTo a stirring solution of 5-hydroxy-3,4-dihydroisoquinolin-1(2H)-one (200 mg, 1.226 mmol) in DMF (8 ml) was added Cs2C03 (599 mg, 1.839 mmol). The reation mixture was left to stir for 20 minutes at 50 C and then treated with methyl iodide (0.115 ml, 1.839 mmol). After stirring at 50 C for 30 min, the mixture was diluted with EtOAc water. The organic portion was separated and washed with water, brine, dried (MgS04) and concentrated in vacuo to afford the title compound as a pale yellow solid; LC-MS Rt =1.08 mins; MS m/z 178.1 [M+H]+; Method 2minLC_v002.
  • 11
  • [ 40731-98-4 ]
  • [ 129075-49-6 ]
  • 12
  • [ 129075-49-6 ]
  • 2-(3-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl)propyl)-5-methoxy-3,4-dihydroisoquinolin-1(2H)-one [ No CAS ]
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