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[ CAS No. 960613-96-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 960613-96-1
Chemical Structure| 960613-96-1
Structure of 960613-96-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 960613-96-1 ]

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Product Details of [ 960613-96-1 ]

CAS No. :960613-96-1 MDL No. :MFCD11520857
Formula : C6H3BrClN3 Boiling Point : -
Linear Structure Formula :- InChI Key :IYSBSUPWYUVHKG-UHFFFAOYSA-N
M.W : 232.47 Pubchem ID :45480507
Synonyms :

Calculated chemistry of [ 960613-96-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.7
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) : -6.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.87
Log Po/w (XLOGP3) : 1.98
Log Po/w (WLOGP) : 2.15
Log Po/w (MLOGP) : 1.95
Log Po/w (SILICOS-IT) : 1.8
Consensus Log Po/w : 1.95

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.13
Solubility : 0.171 mg/ml ; 0.000734 mol/l
Class : Soluble
Log S (Ali) : -2.24
Solubility : 1.34 mg/ml ; 0.00576 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.19
Solubility : 0.15 mg/ml ; 0.000647 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.77

Safety of [ 960613-96-1 ]

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 [ 960613-96-1 ]

* 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.

  • Downstream synthetic route of [ 960613-96-1 ]

[ 960613-96-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 960613-96-1 ]
  • [ 893440-50-1 ]
  • [ 199609-62-6 ]
  • [ 1414463-32-3 ]
YieldReaction ConditionsOperation in experiment
63% Reaction performed in parallel in 7 batches of 500 mg of 6 in a carrousel. From 3-bromo-5-chloropyrazolo[1,5-a]pyrimidine (6) (500 mg, 2.151 mmol), (5-amino-6-methoxypyridin-3-yl)boronic acid pinacol ester (538 mg, 2.151 mmol,), PdCl2(PPh3)2 (75 mg) in 1,2-DME (9 mL) and Na2CO3 (aq sat sol, 4.3 mL) heated at 80 C in semi-pressure tubes for 30 min. Then <strong>[199609-62-6]3-(N-Boc-aminomethyl)phenylboronic acid</strong> (675 mg, 2.689 mmol,) PdCl2(PPh3)2 (45 mg) were added and the mixture was heated at 100 C for 5 h. Purification of all batches together using gradient from 0% to 100% of EtOAc in cHex afforded 20 (4.23 g, 63%). LCMS (ESI): Rt = 4.68 min, m/z = 447.10 [M+ H]+.
  • 2
  • [ 960613-96-1 ]
  • [ 143238-38-4 ]
  • [ 1454558-26-9 ]
  • 3
  • [ 960613-96-1 ]
  • [ 143238-38-4 ]
  • C21H25N5O2 [ No CAS ]
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