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[ CAS No. 473932-16-0 ] 2-(Quinoxalin-6-yl)acetic acid

Cat. No.: A432730
Chemical Structure| 473932-16-0
Chemical Structure| 473932-16-0
Structure of 473932-16-0 * Storage: Sealed in dry,2-8°C

Quality Control of [ 473932-16-0 ]

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Product Details of [ 473932-16-0 ]

CAS No. :473932-16-0 MDL No. :MFCD09880609
Formula : C10H8N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NRRFVLPMUSJDJY-UHFFFAOYSA-N
M.W : 188.18 Pubchem ID :18436916
Synonyms :

Calculated chemistry of [ 473932-16-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 10
Fraction Csp3 : 0.1
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.08
TPSA : 63.08 Ų

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) : -6.97 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.19
Log Po/w (XLOGP3) : 0.67
Log Po/w (WLOGP) : 1.26
Log Po/w (MLOGP) : 0.49
Log Po/w (SILICOS-IT) : 1.62
Consensus Log Po/w : 1.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.83
Solubility : 2.81 mg/ml ; 0.0149 mol/l
Class : Very soluble
Log S (Ali) : -1.57
Solubility : 5.05 mg/ml ; 0.0268 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.11
Solubility : 0.147 mg/ml ; 0.00078 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.48

Safety of [ 473932-16-0 ]

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

Application In Synthesis of [ 473932-16-0 ]

* 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 [ 473932-16-0 ]

[ 473932-16-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 473932-16-0 ]
  • [ 18107-18-1 ]
  • [ 1233318-23-4 ]
YieldReaction ConditionsOperation in experiment
In methanol; hexanes; toluene; Trimethylsilyldiazomethane [2.0M in hexanes] (0.08?xL) was added dropwise to a solution of quinoxalin-6-yl-acetic acid (0.030g, 0.159mmol) in toluene/methanol [8/1] (0.5mL) and stirred until the bubbling stopped. The reaction was then evaporated and the crude product was purified via silica gel column chromatography in hexane: ethyl acetate (1:1) to give 0.013g of quinoxaJin-6-yl-acetic acid methyl ester. This was added to a solution of hydrazine (O.lOinL) in methanol and stirred at room temperature overnight. The reaction mixture was evaporated in vacuo to give 0.019g of quinoxalin-6-yl-acetic acid hydrazide. 1H NMR (400 MHz, DMSO-d6) 8 9.77 (bs, IH), 9.35 (m, 2H), 8.46 (d, IH, J=8.8Hz), 8.39 (m, IH), 8.19 (dd, IH, J=2.0, 8.8Hz), 4.68 (bs, 2H), 4.07 (s, 2H).
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