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[ CAS No. 162046-66-4 ] {[proInfo.proName]}

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Chemical Structure| 162046-66-4
Chemical Structure| 162046-66-4
Structure of 162046-66-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 162046-66-4 ]

CAS No. :162046-66-4 MDL No. :MFCD04115067
Formula : C16H22N2O4 Boiling Point : -
Linear Structure Formula :- InChI Key :BEDWYXZFIYMEJG-UHFFFAOYSA-N
M.W : 306.36 Pubchem ID :2795508
Synonyms :
Chemical Name :4-(4-(tert-Butoxycarbonyl)piperazin-1-yl)benzoic acid

Calculated chemistry of [ 162046-66-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 22
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.5
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 90.6
TPSA : 70.08 ?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) : -6.59 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.74
Log Po/w (XLOGP3) : 2.23
Log Po/w (WLOGP) : 1.68
Log Po/w (MLOGP) : 1.8
Log Po/w (SILICOS-IT) : 1.12
Consensus Log Po/w : 1.91

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.02
Solubility : 0.295 mg/ml ; 0.000964 mol/l
Class : Soluble
Log S (Ali) : -3.34
Solubility : 0.141 mg/ml ; 0.00046 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.44
Solubility : 1.11 mg/ml ; 0.00364 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.34

Safety of [ 162046-66-4 ]

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

Application In Synthesis of [ 162046-66-4 ]

* 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 [ 162046-66-4 ]

[ 162046-66-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 162046-66-4 ]
  • [ 5369-19-7 ]
  • [ 1224871-16-2 ]
YieldReaction ConditionsOperation in experiment
35% With dmap; In dichloromethane; at 20℃; Example 163 4-[4-(3-tert-Butyl-phenylcarbamoyl)-phenyl]-piperazine-1-carboxylic acid tert-butyl ester A mixture of 3-tert-butyl aniline (117 mg, 0.78 mmol), 4-(4-carboxy-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (prepared as described in ) (200 mg, 0.65 mmol), EDCI (375 mg, 0.95 mmol) and a catalytic amount of DMAP in CH2Cl2 was stirred at room temperature overnight. The next day the mixture was partitioned between EtOAc and water. The organic layer was collected, dried over Na2SO4, filtered and concentrated. The residue was chromatographed with silica gel column amd 0-30percent EtOAc in hexanes gradient to afford the product (100 mg, Yield: 35percent). HRMS m/z calcd for C26H35N3O3 [M+H]+: 438.2751; Found: 438.2753.
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