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[ CAS No. 95656-86-3 ] {[proInfo.proName]}

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Chemical Structure| 95656-86-3
Chemical Structure| 95656-86-3
Structure of 95656-86-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 95656-86-3 ]

CAS No. :95656-86-3 MDL No. :MFCD02093569
Formula : C8H17NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YNJCFDAODGKHAV-UHFFFAOYSA-N
M.W : 175.23 Pubchem ID :9920508
Synonyms :

Calculated chemistry of [ 95656-86-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.88
Num. rotatable bonds : 5
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 46.25
TPSA : 58.56 ?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) : -6.89 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.19
Log Po/w (XLOGP3) : 0.68
Log Po/w (WLOGP) : 0.89
Log Po/w (MLOGP) : 0.63
Log Po/w (SILICOS-IT) : 0.2
Consensus Log Po/w : 0.92

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.02
Solubility : 16.6 mg/ml ; 0.0945 mol/l
Class : Very soluble
Log S (Ali) : -1.49
Solubility : 5.71 mg/ml ; 0.0326 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.09
Solubility : 14.1 mg/ml ; 0.0805 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.61

Safety of [ 95656-86-3 ]

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

Application In Synthesis of [ 95656-86-3 ]

* 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 [ 95656-86-3 ]

[ 95656-86-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 95656-86-3 ]
  • [ 170384-29-9 ]
YieldReaction ConditionsOperation in experiment
61% With dipyridinium dichromate; In N,N-dimethyl-formamide; at 0 - 23℃; for 16h;Inert atmosphere; To a solution of PDC (68.9 g, 183 mmol) in DMF (50 mL) was added 45 (16.0 g, 92.0 mmol) in DMF (42 mL) at 0 C. The reaction was allowedto stir for 16 h while warming to 23 C. The reaction mixture waspoured over a plug of Celite with Et2O, quenched with brine (200 mL),and diluted with Et2O (700 mL). The combined Et2O layers werewashed with aq NH4Cl (2 × 200 mL), H2O (2 × 200 mL), and brine(2 × 200 mL), dried (MgSO4), filtered, and concentrated to give Boc-aminoacetone 42 as a yellow oil; yield: 10.6 g (61.0 mmol, 61%).
52% With sulfur trioxide pyridine complex; triethylamine; In dichloromethane; dimethyl sulfoxide; for 6h; 2.24 g (12.7 mmol) of (2-hydroxy-propyl)-carbamic acid t-butyl ester obtained in the above step (1) was dissolved in 30 mL of dichloromethane, and then 3.6 mL (25.7 mmol) of triethylamine was dropwise added. To the resulting solution, was added a solution of 6.05 g (19 mmol) of 50% pyridine sulfur trioxide which was dissolved in 15 mL of dimethylsulf oxide. After 6 hours, 200 mL of ethyl acetate was added thereto and the reaction solution was washed with water, then an organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, then the residue was purified by column chromatography to give 1.15 g (6.64 mmol) of the title compound in a yield of 52%.[376] NMR: 1H-NMR(CDCl3) delta 5.2O(1H, brs), 4.05~4.00(2H, m), 2.17(3H, s), 1.43(9H, s)[377] Mass(EI) 174(M++.)
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