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[ CAS No. 250275-15-1 ] {[proInfo.proName]}

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Chemical Structure| 250275-15-1
Chemical Structure| 250275-15-1
Structure of 250275-15-1 * Storage: {[proInfo.prStorage]}

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Product Details of [ 250275-15-1 ]

CAS No. :250275-15-1 MDL No. :MFCD04116224
Formula : C11H20N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :FYUVLZRRIRGSTE-DTORHVGOSA-N
M.W : 212.29 Pubchem ID :1514452
Synonyms :

Calculated chemistry of [ 250275-15-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.91
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 66.0
TPSA : 41.57 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.07 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.59
Log Po/w (XLOGP3) : 0.74
Log Po/w (WLOGP) : 0.31
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : 0.65
Consensus Log Po/w : 1.09

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.42
Solubility : 7.99 mg/ml ; 0.0376 mol/l
Class : Very soluble
Log S (Ali) : -1.19
Solubility : 13.6 mg/ml ; 0.0643 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.37
Solubility : 8.97 mg/ml ; 0.0423 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.99

Safety of [ 250275-15-1 ]

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

Application In Synthesis of [ 250275-15-1 ]

* 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 [ 250275-15-1 ]

[ 250275-15-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 60211-57-6 ]
  • [ 530-62-1 ]
  • [ 250275-15-1 ]
  • (3aR,6aS)-2-tert-butyl 5-(3,5-dichlorobenzyl) tetrahydropyrrolo[3,4-c]pyrrole-2,5(1H,3H)-dicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
99% To a light brown solution of <strong>[60211-57-6](3,5-dichlorophenyl)methanol</strong> (425 mg, 2.35 mmol) in dichloromethane (7 rriL) was added N,N'-carbonyldiimidazole (401 mg, 2.47 mmol). The solution was stirred at room temperature for 3 h, then (3aR,6aS)-tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(lH)-carboxylate (CAS-RN 250275-15-1 ; 526 mg, 2.35 mmol) was added, then after 15 h the reaction mixture was partitioned between 1 M aq. hydrochloric acid solution and dichloromethane. The organic layer was washed with brine, dried over magnesium sulfate, filtered and evaporated to afford the title compound (972 mg, 99%). Light brown viscous oil, MS: 359.2 (M-C(CH3)3+H)+.
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