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[ CAS No. 14793-00-1 ] {[proInfo.proName]}

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Chemical Structure| 14793-00-1
Chemical Structure| 14793-00-1
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Product Details of [ 14793-00-1 ]

CAS No. :14793-00-1 MDL No. :MFCD07778346
Formula : C7H6ClN3 Boiling Point : -
Linear Structure Formula :- InChI Key :GWHLOBFYCUGPGE-UHFFFAOYSA-N
M.W : 167.60 Pubchem ID :10442072
Synonyms :

Calculated chemistry of [ 14793-00-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.14
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.96
TPSA : 30.19 ?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) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.89
Log Po/w (XLOGP3) : 1.69
Log Po/w (WLOGP) : 1.69
Log Po/w (MLOGP) : 1.52
Log Po/w (SILICOS-IT) : 1.54
Consensus Log Po/w : 1.67

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.55
Solubility : 0.473 mg/ml ; 0.00282 mol/l
Class : Soluble
Log S (Ali) : -1.94
Solubility : 1.93 mg/ml ; 0.0115 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.71
Solubility : 0.328 mg/ml ; 0.00195 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.12

Safety of [ 14793-00-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 14793-00-1 ]

* 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 [ 14793-00-1 ]

[ 14793-00-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 14793-00-1 ]
  • [ 18112-31-7 ]
YieldReaction ConditionsOperation in experiment
90% With N-Bromosuccinimide In chloroform at 20℃; for 15 h; Preparation of 3-bromo-6-chloro-2-methylimidazo[1,2-b]pyridazine
To a solution of 6-chloro-2-methylimidazo[1,2-b]pyridazine (2.00 g, 11.9 mmol, 1.0 equiv) in chloroform (50 mL) was added N-bromosuccinimide (2.55 g, 14.3 mmol, 1.2 equiv).
The reaction was stirred at room temperature for 15 h.
Purification by column chromatography using 50percent ethyl acetate in hexanes elution gave 2.64 g of the yellow solid, 90percent.
Reference: [1] Patent: US2014/256733, 2014, A1, . Location in patent: Paragraph 0266; 0269-0270
[2] Patent: WO2008/52733, 2008, A1, . Location in patent: Page/Page column 81
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