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[ CAS No. 169280-83-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 169280-83-5
Chemical Structure| 169280-83-5
Structure of 169280-83-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 169280-83-5 ]

CAS No. :169280-83-5 MDL No. :MFCD07186264
Formula : C11H16N2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BORDVYKLAFQRSP-UHFFFAOYSA-N
M.W : 224.26 Pubchem ID :3575389
Synonyms :

Calculated chemistry of [ 169280-83-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.45
Num. rotatable bonds : 5
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 60.61
TPSA : 71.45 ?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) : -7.06 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 0.86
Log Po/w (WLOGP) : 1.58
Log Po/w (MLOGP) : 0.7
Log Po/w (SILICOS-IT) : 1.04
Consensus Log Po/w : 1.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.72
Solubility : 4.28 mg/ml ; 0.0191 mol/l
Class : Very soluble
Log S (Ali) : -1.94
Solubility : 2.55 mg/ml ; 0.0114 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.81
Solubility : 0.344 mg/ml ; 0.00153 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.35

Safety of [ 169280-83-5 ]

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

Application In Synthesis of [ 169280-83-5 ]

* 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 [ 169280-83-5 ]

[ 169280-83-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 199296-40-7 ]
  • [ 169280-83-5 ]
  • 2
  • [ 169280-83-5 ]
  • [ 199296-40-7 ]
YieldReaction ConditionsOperation in experiment
With pyridine-SO3 complex; dimethyl sulfoxide; triethylamine; at 20℃; Production Example 1 To a mixture of tert-butyl [5-(hydroxymethyl)pyridine-2-yl]carbamate (2.13 g), triethylamine (5.3 ml), and DMSO (15 ml), a sulfur trioxide-pyridine complex (3.02 g) in a DMSO solution (15 ml) was added dropwise, followed by stirring at room temperature for 4.5 hours. To the reaction mixture, water was added, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After removing the desiccant, the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.00 g of tert-butyl (5-formylpyridin-2-yl)carbamate.
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