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[ CAS No. 51984-46-4 ] {[proInfo.proName]}

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Chemical Structure| 51984-46-4
Chemical Structure| 51984-46-4
Structure of 51984-46-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 51984-46-4 ]

CAS No. :51984-46-4 MDL No. :MFCD08234494
Formula : C7H9NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :RDXXAIGOEPIQPK-UHFFFAOYSA-N
M.W : 139.15 Pubchem ID :5324774
Synonyms :

Calculated chemistry of [ 51984-46-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.29
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.86
TPSA : 42.35 ?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) : -7.17 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.61
Log Po/w (XLOGP3) : -0.03
Log Po/w (WLOGP) : 0.43
Log Po/w (MLOGP) : -0.39
Log Po/w (SILICOS-IT) : 1.17
Consensus Log Po/w : 0.56

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.0
Solubility : 14.0 mg/ml ; 0.101 mol/l
Class : Very soluble
Log S (Ali) : -0.41
Solubility : 54.2 mg/ml ; 0.39 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.95
Solubility : 1.55 mg/ml ; 0.0111 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.57

Safety of [ 51984-46-4 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 51984-46-4 ]

* 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 [ 51984-46-4 ]

[ 51984-46-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14173-30-9 ]
  • [ 74-88-4 ]
  • [ 51984-46-4 ]
YieldReaction ConditionsOperation in experiment
7% With potassium hydroxide; In water; dimethyl sulfoxide; a 3-Methoxy(2-hydroxymethyl)pyridine To a mixture of ground potassium hydroxide (10.2 g, 0.186 mol) in dimethylsulphoxide (15 ml) under nitrogen was added 3-hydroxy(2-hydroxymethyl)pyridine hydrochloride (5.0 g, 0.031 mol) in dimethylsulphoxide (15 ml) over 0.25 h. The reaction was stirred at room temperature for 1 h before the addition of methyl iodide (1.92 ml, 0.0309 mol) and then stirred at room temperature overnight. Water (100 ml) was added and the solution acidified to pH 1 with 2N hydrochloric acid, washed with dichloromethane (*3) and then basified with solid potassium carbonate until pH 12 was attained. The aqueous was extracted with dichloromethane (*3), dried (MgSO4), evaporated in vacuo and the residue purified by chromatography on silica gel, eluding with dichloromethane/methanol/ammonia (90:5:0.5), to give the title-compound (300 mg, 7%). 1H NMR (360 MHz, CDCl3) δ 3.85 (3H, s, CH3), 4.74 (2H, s, CH2), 7.12 (1H, d, J=8.3 Hz, Ar-H), 7.21 (1H, m, Ar-H), 8.15 (1H, d, J=4.8 Hz, Ar-H).
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