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[ CAS No. 105250-17-7 ] {[proInfo.proName]}

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Chemical Structure| 105250-17-7
Chemical Structure| 105250-17-7
Structure of 105250-17-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 105250-17-7 ]

CAS No. :105250-17-7 MDL No. :MFCD03791261
Formula : C6H8N2O Boiling Point : -
Linear Structure Formula :- InChI Key :ZRJJXXDQIQFZBW-UHFFFAOYSA-N
M.W : 124.14 Pubchem ID :1515296
Synonyms :

Calculated chemistry of [ 105250-17-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 34.77
TPSA : 59.14 ?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) : -7.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.02
Log Po/w (XLOGP3) : -0.69
Log Po/w (WLOGP) : 0.01
Log Po/w (MLOGP) : -0.34
Log Po/w (SILICOS-IT) : 0.49
Consensus Log Po/w : 0.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.6
Solubility : 31.0 mg/ml ; 0.25 mol/l
Class : Very soluble
Log S (Ali) : -0.08
Solubility : 104.0 mg/ml ; 0.837 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.45
Solubility : 4.39 mg/ml ; 0.0354 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.31

Safety of [ 105250-17-7 ]

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 [ 105250-17-7 ]

* 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 [ 105250-17-7 ]

[ 105250-17-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 33142-21-1 ]
  • [ 105250-17-7 ]
  • ethyl 7-(hydroxymethyl)imidazo[1,2-a]pyridine-3-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
47% In tert-butyl alcohol; at 75℃; for 4h;Inert atmosphere; Ethyl 7-(hydroxymethyl)imidazo[1,2-a]pyridine-3-carboxylate (3) A mixture of (2-aminopyridin-4-yl)methanol (1, 149 mg, 1.20 mmol) and <strong>[33142-21-1]ethyl 2-chloro-3-oxopropanoate</strong> (2, 144 mg, 0.956 mmol), in t-butanol (3 ml), was stirred at 75 C. under N2 for 4 h. After cooling down to room temperature, solvent was evaporated, and the residue was further purified with flash silica gel column, with EA/Hex (gradient up to 99:1), to provide the product as white solid (98 mg, 47%). 1H NMR (500 MHz, Chloroform-d) delta 9.04 (dd, J=7.0, 0.9 Hz, 1H), 8.08 (s, 1H), 7.63 (t, J=1.4 Hz, 1H), 6.91 (dd, J=7.1, 1.7 Hz, 1H), 4.71 (d, J=1.3 Hz, 2H), 4.32 (q, J=7.1 Hz, 2H), 1.34 (t, J=7.2 Hz, 3H); 13C NMR (126 MHz, Chloroform-d) delta 160.43, 148.28, 143.42, 140.81, 127.06, 115.67, 113.44, 113.34, 62.91, 60.49, 14.40; ESIMS m/z 221.5 [MH]+.
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