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[ CAS No. 1452561-74-8 ] {[proInfo.proName]}

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Chemical Structure| 1452561-74-8
Chemical Structure| 1452561-74-8
Structure of 1452561-74-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1452561-74-8 ]

CAS No. :1452561-74-8 MDL No. :MFCD31744070
Formula : C9H10ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :YNCYUAQQSCDCMZ-UHFFFAOYSA-N
M.W : 199.63 Pubchem ID :86694110
Synonyms :

Calculated chemistry of [ 1452561-74-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.29
TPSA : 50.19 Ų

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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.51
Log Po/w (XLOGP3) : 2.21
Log Po/w (WLOGP) : 2.1
Log Po/w (MLOGP) : 1.28
Log Po/w (SILICOS-IT) : 2.03
Consensus Log Po/w : 1.83

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -2.68
Solubility : 0.418 mg/ml ; 0.00209 mol/l
Class : Soluble
Log S (Ali) : -2.9
Solubility : 0.252 mg/ml ; 0.00126 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.84
Solubility : 0.287 mg/ml ; 0.00144 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 1452561-74-8 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501 UN#:2811
Hazard Statements:H301-H311-H331 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1452561-74-8 ]

* 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 [ 1452561-74-8 ]

[ 1452561-74-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 871014-19-6 ]
  • [ 1452561-74-8 ]
  • [ 1452560-42-7 ]
YieldReaction ConditionsOperation in experiment
86% With 2-(1H-9-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate; triethylamine; In dichloromethane; at 20℃; for 21h; 2-(2-Chloropyridin-3-yl)-2-methylpropanoic acid hydrochloride (intermediate 25, 992 mg, 4.20 mmol), tert-butyl(trans-3-aminocyclobutyl)carbamate (939 mg, 5.04 mmol), hatu (2077 mg, 5.46 mmol) and triethylamine (2.4 ml, 16.81 mmol) were dissolved in dichloromethane (8.4 mL). The reaction mixture was stirred at room temperature for 21 hours then diluted with water and extracted with dichloromethane. The organic was washed with saturated ammonium chloride and dried over magnesium sulfate. Evaporation under reduced pressure and purification using silica chromatography (0% to 100% ethyl acetate in hexane gradient) gave tert-butyl(trans-3-(2-(2-chloropyridin-3-yl)-2-methylpropanamido)cyclobutyl)carbamate (1327 mg, 3.61 mmol, 86% yield) as white solid.
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