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[ CAS No. 24812-90-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 24812-90-6
Chemical Structure| 24812-90-6
Structure of 24812-90-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 24812-90-6 ]

CAS No. :24812-90-6 MDL No. :MFCD00017196
Formula : C9H11NO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :QVDWKLDUBSJEOG-UHFFFAOYSA-N
M.W : 181.19 Pubchem ID :2734814
Synonyms :

Calculated chemistry of [ 24812-90-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 3
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.62
TPSA : 61.55 ?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) : -6.64 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.95
Log Po/w (XLOGP3) : 1.08
Log Po/w (WLOGP) : 1.07
Log Po/w (MLOGP) : 1.06
Log Po/w (SILICOS-IT) : 0.99
Consensus Log Po/w : 1.23

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.79
Solubility : 2.96 mg/ml ; 0.0163 mol/l
Class : Very soluble
Log S (Ali) : -1.96
Solubility : 1.97 mg/ml ; 0.0109 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.24
Solubility : 1.04 mg/ml ; 0.00573 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 24812-90-6 ]

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

Application In Synthesis of [ 24812-90-6 ]

* 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 [ 24812-90-6 ]

[ 24812-90-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 40757-20-8 ]
  • [ 24812-90-6 ]
YieldReaction ConditionsOperation in experiment
With hydrogen;Raney nickel; In N,N-dimethyl-formamide; under 2585.81 Torr; for 5.0h; INTERMEDIATE 1; 4-methoxy-acridine-l-carboxyIic acid; STEP 1: Methyl-(3-amino-4-methoxy) benzoate; Methyl (4-methoxy-3-nitro)benzoate (4.2 g, 0.019 mol) (Lancaster) was dissolved in DMF (65 ml) and hydrogenated in the presence of Raney nickel (2.1 g) for 5 h at 50 psi. The reaction mixture was filtered through celite. Water (100 ml) was added to the filtrate to precipitate the product. The precipitated product was extracted in dichloromethane, dried over anhydrous sodium sulphate, and concentrated in vacuo to obtain the product as a buff color solid (3.4 g).IR (KBr): 3297, 2949, 2846, 1710, 1600, 1517, 1440, 1310, 1219, 1198, 1106, 1021, 876, 761 cm"1. H*-NMR (300 MHz, DMSOd6) delta 3.76 (s, 3 H), 3.82 (s, 3 H), 4.99 (brs, 2 H, exchanges with D2O), 6.87 (d, 1 H, J = 8.4 Hz), 7.21 (d, 1 H, J = 8.2 Hz), 7.26 (s, IH).
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