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[ CAS No. 1422-53-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1422-53-3
Chemical Structure| 1422-53-3
Structure of 1422-53-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1422-53-3 ]

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Product Details of [ 1422-53-3 ]

CAS No. :1422-53-3 MDL No. :MFCD00040828
Formula : C7H6BrF Boiling Point : No data available
Linear Structure Formula :BrC6H3(CH3)F InChI Key :SFGFOJPGCOYQJK-UHFFFAOYSA-N
M.W : 189.03 Pubchem ID :74016
Synonyms :

Calculated chemistry of [ 1422-53-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 0.0
Molar Refractivity : 39.07
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
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) : -5.27 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.28
Log Po/w (XLOGP3) : 3.08
Log Po/w (WLOGP) : 3.32
Log Po/w (MLOGP) : 3.79
Log Po/w (SILICOS-IT) : 3.4
Consensus Log Po/w : 3.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.45
Solubility : 0.0677 mg/ml ; 0.000358 mol/l
Class : Soluble
Log S (Ali) : -2.75
Solubility : 0.338 mg/ml ; 0.00179 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.92
Solubility : 0.0228 mg/ml ; 0.000121 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.19

Safety of [ 1422-53-3 ]

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

Application In Synthesis of [ 1422-53-3 ]

* 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 [ 1422-53-3 ]

[ 1422-53-3 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1422-53-3 ]
  • [ 174603-55-5 ]
  • 2
  • [ 1422-53-3 ]
  • [ 137466-14-9 ]
  • 5
  • [ 1422-53-3 ]
  • [ 124-38-9 ]
  • [ 1359857-60-5 ]
YieldReaction ConditionsOperation in experiment
85% 300 mL dry THF was charged to an oven dried 1000 mL three neck RBF fitted with two septa and a nitrogen inlet. A solution of diisopropylamine (20.0 ml, 142 mmol) in THF (300 mL) was in an ice/water bath. n-butyllithium (45 ml, 113 mmol) solution was added slowly and stirred at 0 C. for an additional 15 minutes before cooling in an iPrOH/CO2 bath. 2-bromo-4-fluoro-1-methylbenzene (12 ml, 97 mmol) was added slowly over 10 minutes and stirred cold for 1 hour before carbon dioxide was bubbled through the mixture. After 20 minutes bubbling while cold, the reaction was allowed to warm to room temperature while still bubbling, after which 100 mL of water was added. The organic layer was extracted with 3×100 mL 0.1M aq. NaOH. Combined water layers were washed with EtOAc and acidified to pH 1 with 6M HCl. Extraction with EtOAc, drying and condensation under reduced pressure afforded 19.24 g (85%) of the (14).
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