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[ CAS No. 436799-33-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 436799-33-6
Chemical Structure| 436799-33-6
Structure of 436799-33-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 436799-33-6 ]

CAS No. :436799-33-6 MDL No. :MFCD04972700
Formula : C6H3BrF3N Boiling Point : -
Linear Structure Formula :- InChI Key :HEDHNDVPKRVQPN-UHFFFAOYSA-N
M.W : 225.99 Pubchem ID :11127991
Synonyms :

Calculated chemistry of [ 436799-33-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.94
TPSA : 12.89 ?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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.85
Log Po/w (XLOGP3) : 2.43
Log Po/w (WLOGP) : 4.02
Log Po/w (MLOGP) : 2.33
Log Po/w (SILICOS-IT) : 3.05
Consensus Log Po/w : 2.73

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.11
Solubility : 0.176 mg/ml ; 0.000777 mol/l
Class : Soluble
Log S (Ali) : -2.34
Solubility : 1.02 mg/ml ; 0.00453 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.77
Solubility : 0.0383 mg/ml ; 0.000169 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.66

Safety of [ 436799-33-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 436799-33-6 ]

* 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 [ 436799-33-6 ]

[ 436799-33-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 885069-14-7 ]
  • [ 436799-33-6 ]
  • [ 1190784-05-4 ]
YieldReaction ConditionsOperation in experiment
56.4% With caesium carbonate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In water; dimethyl sulfoxide; at 110℃; for 3h;Inert atmosphere; As shown in step 3-i of Scheme 3, 3-bromo-5-(trifluoromethyl)pyridine (2.0 g, 8.85 mmol) and N-[6-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)-l,3-benzothiazol-2- yljacetamide (4.23 g, 13.3 mmol) were combined in DMSO (60.0 mL) and stirred. Once the reagents had dissolved, CS2CO3 (8.65 g, 26.55 mmol) was added, followed by addition of water (12.0 mL). The reaction mixture was flushed with nitrogen gas for 30 min. and Pd(dppf)Cl2 (648 g, 0.885 mmol) was added. The reaction was heated at HO0C for 3 hours. After the reaction mixture was cooled to room temperature a precipitate formed, which was filtered off in a Buchner funnel to provide lambda/-(6-(5-(trifluoromethyl)pyridin-3- yl)benzo[
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