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[ CAS No. 186407-74-9 ] {[proInfo.proName]}

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Chemical Structure| 186407-74-9
Chemical Structure| 186407-74-9
Structure of 186407-74-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 186407-74-9 ]

CAS No. :186407-74-9 MDL No. :MFCD05664001
Formula : C7H5BrN2 Boiling Point : -
Linear Structure Formula :- InChI Key :KJIODOACRIRBPB-UHFFFAOYSA-N
M.W : 197.03 Pubchem ID :22352548
Synonyms :

Calculated chemistry of [ 186407-74-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.79
TPSA : 28.68 ?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) : -5.91 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.28
Log Po/w (XLOGP3) : 2.24
Log Po/w (WLOGP) : 2.33
Log Po/w (MLOGP) : 1.88
Log Po/w (SILICOS-IT) : 2.75
Consensus Log Po/w : 2.1

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.14
Solubility : 0.143 mg/ml ; 0.000726 mol/l
Class : Soluble
Log S (Ali) : -2.48
Solubility : 0.656 mg/ml ; 0.00333 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.77
Solubility : 0.0337 mg/ml ; 0.000171 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.51

Safety of [ 186407-74-9 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P301+P310+P330-P302+P352-P305+P351+P338 UN#:2811
Hazard Statements:H301-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 186407-74-9 ]

* 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 [ 186407-74-9 ]

[ 186407-74-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 885069-14-7 ]
  • [ 186407-74-9 ]
  • [ 1112980-20-7 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,4-dioxane; water; at 95℃; Example 99; <n="73"/>N-(6-(1H-Indazol-4-yl)benzo[d]thiazol-2-yl)acetamide; 4-Bromo-1H-indazole (96.8 mg, 0.491 mmol), N-(6-(4,4,5,5-tetramethyl-l ,3,2-dioxaborolan-2- yl)benzo[d]thiazol-2-yl)acetamide (193.2 mg, 6.072 mmol), and tetrakis(triphenylphosphine)palladium(0) (51.5 mg, 44.6 mumol) were suspended in 1 ,4-dioxane (2.0 mL) and sodium carbonate (0.50 mL, 2M in water, 1.0 mmol) was added. The flask was fit with a reflux condensor and placed in a preheated oil bath (95 C) and stirred under nitrogen overnight. The mixture was then cooled to RT and filtered through a pad of Celite(diatomaceous earth). The filtrate was concentrated and purified on HPLC ( 10- 95% MeCN / water with 0.1% TFA over 40 minutes) to give N-(6-(1H-indazol-4-yl)benzo[d]thiazol-2- yl)acetamide. MS (ESI pos. ion) m/z: 309 (MH+). Calculated exact mass for C16H12N4OS: 308.
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