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[ CAS No. 38025-90-0 ] {[proInfo.proName]}

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Chemical Structure| 38025-90-0
Chemical Structure| 38025-90-0
Structure of 38025-90-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 38025-90-0 ]

CAS No. :38025-90-0 MDL No. :MFCD09757508
Formula : C6H4ClNO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BSCFFOOWFVZSSK-UHFFFAOYSA-N
M.W : 173.55 Pubchem ID :29919580
Synonyms :

Calculated chemistry of [ 38025-90-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 38.23
TPSA : 70.42 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.42 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.95
Log Po/w (XLOGP3) : 1.32
Log Po/w (WLOGP) : 1.14
Log Po/w (MLOGP) : -0.69
Log Po/w (SILICOS-IT) : 0.92
Consensus Log Po/w : 0.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.09
Solubility : 1.43 mg/ml ; 0.00822 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.691 mg/ml ; 0.00398 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.44
Solubility : 6.36 mg/ml ; 0.0366 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.69

Safety of [ 38025-90-0 ]

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 [ 38025-90-0 ]

* 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.

  • Upstream synthesis route of [ 38025-90-0 ]
  • Downstream synthetic route of [ 38025-90-0 ]

[ 38025-90-0 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 38496-18-3 ]
  • [ 38025-90-0 ]
YieldReaction ConditionsOperation in experiment
88% at 129℃; for 4 h; Step a 2-chloro-6-oxo-1 ,6-dιhydropyrιdιne-3-carboxylιc acιd; ° A 500-mL round-bottom flask was charged with 2,6-dιchloronιcotιnιc acid (25 0 g 130 mmol), NaOH solution (325 ml_, 2N) and the solution was refluxed at 1290C for 4 hours The reaction mixture was cooled to room temperature and acidified with a 6N aq HCI solution The resulting precipitate was filtered and dried under reduced pressure yielding to the desired product (19 87g, 88percent)
4 g
Stage #1: at 120℃; for 4 h; Inert atmosphere
Stage #2: With hydrogenchloride In water at 20℃;
2,6-Dichloronicotinic acid (6 g) was placed in a 250 mL round bottom flask, and sodium hydroxide solution (80 mL) was added.The mixture was heated to 120 ° C for 4 hours. After the reaction was completed, it was cooled to room temperature, acidified with 6N hydrochloric acid, and the solid was precipitated, filtered, and dried to give the title compound (4 g).
Reference: [1] Patent: WO2010/108652, 2010, A1, . Location in patent: Page/Page column 97
[2] Patent: WO2008/125820, 2008, A1, . Location in patent: Page/Page column 33
[3] Patent: CN108314645, 2018, A, . Location in patent: Paragraph 0094; 0095; 0096; 0097
  • 2
  • [ 262423-77-8 ]
  • [ 38025-90-0 ]
Reference: [1] Patent: US2005/256123, 2005, A1,
[2] Patent: US2005/256123, 2005, A1,
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