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[ CAS No. 24525-63-1 ]

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Chemical Structure| 24525-63-1
Chemical Structure| 24525-63-1
Structure of 24525-63-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 24525-63-1 ]

CAS No. :24525-63-1 MDL No. :MFCD16610775
Formula : C5H3Cl2NO Boiling Point : -
Linear Structure Formula :- InChI Key :BIZWANSOFTWATG-UHFFFAOYSA-N
M.W :163.99 Pubchem ID :57485135
Synonyms :

Calculated chemistry of [ 24525-63-1 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 36.28
TPSA : 33.12 Ų

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) : -6.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.73
Log Po/w (XLOGP3) : 1.79
Log Po/w (WLOGP) : 2.09
Log Po/w (MLOGP) : 1.43
Log Po/w (SILICOS-IT) : 2.23
Consensus Log Po/w : 1.85

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.48
Solubility : 0.546 mg/ml ; 0.00333 mol/l
Class : Soluble
Log S (Ali) : -2.1
Solubility : 1.29 mg/ml ; 0.00787 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.67
Solubility : 0.348 mg/ml ; 0.00212 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.62

Safety of [ 24525-63-1 ]

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 [ 24525-63-1 ]

* 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.

  • Upstream synthesis route of [ 24525-63-1 ]
  • Downstream synthetic route of [ 24525-63-1 ]

[ 24525-63-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 83732-68-7 ]
  • [ 24525-63-1 ]
YieldReaction ConditionsOperation in experiment
89% With hydrogenchloride In water at 150℃; for 0.25 h; Microwave irradiation 2,3-Dichloro-6-methoxypyridine (21 1 mg, 1.19 mmol) and 25percent hydrochloric acid (aq.) (9 imL) was heated in a microwave oven at 150 °C for 15 min and concentrated to dryness in vacuo to afford the product as a pale green solid (173 mg, 89 percent). Data for 2,3-dichloro-6-hydroxypyridine: MS (ESI) m/z: 164/166 ([M+H]+).
89% With hydrogenchloride In water at 150℃; for 0.25 h; 2,3-Dichloro-6-methoxypyridine (211 mg, 1.19 mmol) and 25percent hydrochloric acid (aq.) (9 mL) was heated in a microwave oven at 150 C. for 15 min and concentrated to dryness in vacuo to afford the product as a pale green solid (173 mg, 89percent).Data for 2,3-dichloro-6-hydroxypyridine: MS (ESI) m/z:164/166 ([M+H]+).
Reference: [1] Patent: WO2007/39563, 2007, A1, . Location in patent: Page/Page column 26-27
[2] Patent: US2007/112019, 2007, A1, . Location in patent: Page/Page column 14/1
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