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[ CAS No. 2401-24-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2401-24-3
Chemical Structure| 2401-24-3
Structure of 2401-24-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2401-24-3 ]

CAS No. :2401-24-3 MDL No. :MFCD00047830
Formula : C7H8ClNO Boiling Point : No data available
Linear Structure Formula :- InChI Key :GBOUQGUQUUPGLO-UHFFFAOYSA-N
M.W : 157.60 Pubchem ID :75460
Synonyms :

Calculated chemistry of [ 2401-24-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 42.35
TPSA : 35.25 ?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) : -6.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.82
Log Po/w (XLOGP3) : 1.57
Log Po/w (WLOGP) : 1.94
Log Po/w (MLOGP) : 1.75
Log Po/w (SILICOS-IT) : 1.75
Consensus Log Po/w : 1.76

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.18
Solubility : 1.03 mg/ml ; 0.00654 mol/l
Class : Soluble
Log S (Ali) : -1.92
Solubility : 1.89 mg/ml ; 0.012 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.77
Solubility : 0.268 mg/ml ; 0.0017 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.32

Safety of [ 2401-24-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302+H312-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2401-24-3 ]

* 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 [ 2401-24-3 ]

[ 2401-24-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2401-24-3 ]
  • [ 145742-50-3 ]
  • 2
  • [ 2401-24-3 ]
  • [ 126717-59-7 ]
  • 3,7-dimethoxy-1-methyl-9H-pyrido[3,4-b]indole [ No CAS ]
  • 3
  • [ 2401-24-3 ]
  • [ 126717-59-7 ]
  • N-(2-chloro-5-methoxyphenyl)-6-methoxy-2-methylpyridin-3-amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% With palladium diacetate; caesium carbonate; XPhos; at 100℃; for 15h;Microwave irradiation; Inert atmosphere; <strong>[126717-59-7]3-bromo-6-methoxy-2-methylpyridine</strong> (Aldrich catalog No.758191-1G,0.3 g, 1.485 mmol), 2-(dicyclohexylphosphino)-2',4',6'-tri-i-propyl-1,1'-biphenyl (0.053 g, 0.111 mmol), cesium carbonate (0.581 g, 1.782 mmol) and palladium (II) acetate (0.017 g, 0.074 mmol) were added to a microwave vial. Then, 2-chloro-5-methoxyaniline (Chemimpex catalog No.27675, 0.246 g, 1.559 mmol) was added. The solvent was degassed with argon twice. The reaction was heated on a heating block to 100 C. for 15 hours. The crude reaction mixture was cooled to room temperature and then filtered through celite. The celite was rinsed repeatedly with ethyl acetate to collect the crude product mixture. A reverse-phase column was run (water, acetonitrile) to give N-(2-chloro-5-methoxyphenyl)-6-methoxy-2-methylpyridin-3-amine (0.286 g, 69% yield). 1H NMR (CDCl3, 400 MHz) delta 7.42 (d, 1H, J=8.4 Hz), 7.20 (d, 1H, J=8.4 Hz), 6.60 (d, 1H, J=8.4 Hz), 6.26 (dd, 1H, J=2.8, 8.8 Hz), 6.00 (d, 1H, J=2.8 Hz), 5.65 (s, 1H), 3.93 (s, 3H), 3.66 (s, 3H), 2.37 (s, 3H).
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