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[ CAS No. 125735-40-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 125735-40-2
Chemical Structure| 125735-40-2
Structure of 125735-40-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 125735-40-2 ]

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Product Details of [ 125735-40-2 ]

CAS No. :125735-40-2 MDL No. :MFCD08062427
Formula : C16H16IN Boiling Point : No data available
Linear Structure Formula :- InChI Key :IBCVAYQWXMWFLD-UHFFFAOYSA-N
M.W : 349.21 Pubchem ID :7330610
Synonyms :

Calculated chemistry of [ 125735-40-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 18
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.25
Num. rotatable bonds : 3
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 87.98
TPSA : 3.24 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.43 cm/s

Lipophilicity

Log Po/w (iLOGP) : 3.07
Log Po/w (XLOGP3) : 4.23
Log Po/w (WLOGP) : 3.19
Log Po/w (MLOGP) : 3.93
Log Po/w (SILICOS-IT) : 4.24
Consensus Log Po/w : 3.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.97
Solubility : 0.00378 mg/ml ; 0.0000108 mol/l
Class : Moderately soluble
Log S (Ali) : -4.01
Solubility : 0.0342 mg/ml ; 0.000098 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -5.81
Solubility : 0.000542 mg/ml ; 0.00000155 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.58

Safety of [ 125735-40-2 ]

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

Application In Synthesis of [ 125735-40-2 ]

* 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 [ 125735-40-2 ]

[ 125735-40-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24686-78-0 ]
  • [ 125735-40-2 ]
  • [ 1373356-68-3 ]
YieldReaction ConditionsOperation in experiment
A solution of 1-benzhydryl-3-iodoazetidine 13a (1.4 mmol, 490 mg) in 5 mL of THF was added to a stirring mixture of SmI2 (0.1 M THF solution, 3 mmol, 30 mL) and 1.7 mL of HMPA. After 5 min, a solution of 1-benzoylpiperidin-4-one 13b (3.1 mmol, 626 mg) in 5 mL of THF was added. The reaction mixture was stirred for 2 h. Saturated aqueous NH4Cl solution (20 mL) was added and the suspension was filtered through a diatomaceous earth pad. The solids were washed with chloroform and the combined organic layers were washed with brine, dried, and concentrated. The crude residue was purified by preparative reverse-phase chromatography to give 400 mg (55percent yield) of compound 13c (mono-TFA salt) as a yellow oil. MS m/z 401.2 (M+H+).
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