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[ CAS No. 117482-84-5 ] {[proInfo.proName]}

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Chemical Structure| 117482-84-5
Chemical Structure| 117482-84-5
Structure of 117482-84-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 117482-84-5 ]

CAS No. :117482-84-5 MDL No. :MFCD00015431
Formula : C7H3ClFN Boiling Point : No data available
Linear Structure Formula :- InChI Key :VAHXXQJJZKBZDX-UHFFFAOYSA-N
M.W : 155.56 Pubchem ID :145525
Synonyms :

Calculated chemistry of [ 117482-84-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 36.12
TPSA : 23.79 ?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) : -5.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.77
Log Po/w (XLOGP3) : 2.46
Log Po/w (WLOGP) : 2.77
Log Po/w (MLOGP) : 2.48
Log Po/w (SILICOS-IT) : 2.86
Consensus Log Po/w : 2.47

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.8
Solubility : 0.248 mg/ml ; 0.00159 mol/l
Class : Soluble
Log S (Ali) : -2.6
Solubility : 0.388 mg/ml ; 0.00249 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.36
Solubility : 0.0673 mg/ml ; 0.000433 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.68

Safety of [ 117482-84-5 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P305+P351+P338 UN#:
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 117482-84-5 ]

* 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 [ 117482-84-5 ]

[ 117482-84-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67-56-1 ]
  • [ 117482-84-5 ]
  • [ 102151-33-7 ]
  • 2
  • [ 1196473-37-6 ]
  • [ 117482-84-5 ]
  • [ 1213786-76-5 ]
YieldReaction ConditionsOperation in experiment
33% With potassium carbonate; In dimethyl sulfoxide; at 90℃; for 7h; To a solution of <strong>[1196473-37-6]3H-benzo[c][1,2]oxaborole-1,6-diol</strong> (8) (300?mg, 2.00?mmol) in DMSO (30?mL) were added K2CO3 (828?mg, 6.00?mmol) and 3-chloro-4-fluoro-benzonitrile (7b) (933?mg, 6.00?mmol). The reaction was heated at 90?°C for 7?h. After cooling the reaction mixture to room temperature, EtOAc (50?mL) was added. The organic layer was washed with water (5?×?50?mL). The organic layer was evaporated under vacuum. The residue was purified by reverse phase chromatography to afford 3-chloro-4-(1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-6-yloxy)-benzonitrile (9b) (190?mg, 33percent). 1H NMR (400?MHz, DMSO-d6) delta ppm 9.24 (s, 1H), 8.22 (s, 1H), 7.77 (d, J?=?7.8?Hz, 1H), 7.50 (d, J?=?8.2?Hz, 1H), 7.34 (s, 1H), 7.28 (d, J?=?8.2?Hz, 1H), 7.01 (d, J?=?8.6?Hz, 1H), 4.99 (s, 2H); ESIMS (m/z): 284 (M?H)?; HPLC: 96.4percent (220?nm), 96.0percent (maxplot).
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