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[ CAS No. 254-60-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 254-60-4
Chemical Structure| 254-60-4
Structure of 254-60-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 254-60-4 ]

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Product Details of [ 254-60-4 ]

CAS No. :254-60-4 MDL No. :MFCD00059751
Formula : C8H6N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :FLBAYUMRQUHISI-UHFFFAOYSA-N
M.W : 130.15 Pubchem ID :136069
Synonyms :

Calculated chemistry of [ 254-60-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.54
TPSA : 25.78 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.57 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.32
Log Po/w (XLOGP3) : 2.14
Log Po/w (WLOGP) : 1.63
Log Po/w (MLOGP) : 1.28
Log Po/w (SILICOS-IT) : 2.05
Consensus Log Po/w : 1.68

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.74
Solubility : 0.24 mg/ml ; 0.00184 mol/l
Class : Soluble
Log S (Ali) : -2.31
Solubility : 0.633 mg/ml ; 0.00486 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.29
Solubility : 0.0667 mg/ml ; 0.000513 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.09

Safety of [ 254-60-4 ]

Signal Word:Danger Class:9
Precautionary Statements:P264-P270-P273-P280-P301+P312+P330-P305+P351+P338+P310-P501 UN#:3077
Hazard Statements:H302-H318-H412 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 254-60-4 ]

* 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 [ 254-60-4 ]

[ 254-60-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 254-60-4 ]
  • [ 15992-83-3 ]
YieldReaction ConditionsOperation in experiment
With ammonia; potassium amide; at -40℃; for 3h; A. A solution of [1,8]naphthyridine (0.2 mmol) and potassium amide (0.8 mmol) in liquid ammonia (20 mL) is stirred at -40 C. for 3 h. The solution is concentrated. Residue is partitioned between EtOAc and water. EtOAc layer is separated and washed successively with water and brine. EtOAc layer is dried over sodium sulfate, filtered and concentrated to give [1,8]naphthyridin-2-ylamine which is used as is for the next step.
  • 2
  • [ 7521-41-7 ]
  • [ 815-68-9 ]
  • [ 254-60-4 ]
  • [ 1569-16-0 ]
  • 3
  • [ 254-60-4 ]
  • [ 67-68-5 ]
  • [ 1569-16-0 ]
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