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[ CAS No. 4837-19-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4837-19-8
Chemical Structure| 4837-19-8
Structure of 4837-19-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 4837-19-8 ]

CAS No. :4837-19-8 MDL No. :MFCD00236224
Formula : C8H6F2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :OKKDGIXOKWOMRD-UHFFFAOYSA-N
M.W : 188.13 Pubchem ID :842614
Synonyms :

Calculated chemistry of [ 4837-19-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.0
TPSA : 46.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.34 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.47
Log Po/w (XLOGP3) : 2.97
Log Po/w (WLOGP) : 2.83
Log Po/w (MLOGP) : 1.64
Log Po/w (SILICOS-IT) : 1.64
Consensus Log Po/w : 2.11

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.02
Solubility : 0.179 mg/ml ; 0.000953 mol/l
Class : Soluble
Log S (Ali) : -3.61
Solubility : 0.0461 mg/ml ; 0.000245 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.12
Solubility : 1.43 mg/ml ; 0.00759 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.5

Safety of [ 4837-19-8 ]

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

Application In Synthesis of [ 4837-19-8 ]

* 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 [ 4837-19-8 ]

[ 4837-19-8 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 4837-19-8 ]
  • [ 17114-97-5 ]
  • (2S)-3-(tert-butoxy)-2-[3-(difluoromethoxy)phenyl]formamido}propanoic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
83% To a solution of 3-(difluoromethoxy)benzoic acid (2.82 g, 15 mmol) in DCM (30 mL) was added Et3N (3.34 g, 33 mmol) followed by EDC (3.43 g, 18 mmol) and HOBt (0.27 g, 2 mmol) at room temperature. The reaction mixture was stirred at room temperature for 30 min. Then 0-(tert-butyl)-L- serine methyl ester hydrochloride (3.17 g, 15 mmol) was added and reaction mixture was stirred at room temperature for 12h. Evaporation of solvent under vacuum gave crude residue which was treated with saturated aqueous NaHC03 solution (10 mL), then extracted with ethyl acetate (2 x 100 mL). Dried (Na2S04), filtered and evaporation of solvent under vacuum gave almost pure product as pale yellow syrup which was used as such in the next. Yield : 4.33 g (83percent), LCMS m/z: 346.32 (M+H)+.
  • 2
  • 1-(difluoromethoxy)-3-methyl-6-nitro-4-(trifluoromethyl)-1H-benzo[d][1,2,3]triazol-3-ium trifluoromethanesulfonate [ No CAS ]
  • [ 65-85-0 ]
  • [ 97914-59-5 ]
  • [ 4837-20-1 ]
  • [ 4837-19-8 ]
YieldReaction ConditionsOperation in experiment
With tris(2,2-bipyridine)ruthenium(II) hexafluorophosphate; In acetonitrile; at 23℃; for 12h;Irradiation; Glovebox; Sealed tube; Inert atmosphere; General procedure: In a glovebox, to an oven-dried 20 mL screw cap vial was added 1- (difluoromethoxy) -3-methyl-6-nitro-4- (trifluoromethyl) -lff- benzo [d] [1, 2, 3] triazol-3-ium trifluoromethanesulfonate (la) (92.4 mg, 0.200 mmol, 1.00 equiv), (hetero) arene (2.00 mmol, 10.0 equiv), Ru (bpy) 3 (PF6) 2, (0.860 mg, 1.00 pmol, 0.500 mol%), and MeCM (1.00 mL, 0.200 M, with respect to la) . To this suspension or solution was added a magnetic stir bar. Next, the reaction vial was capped and taken out of the glovebox. The reaction mixture was stirred at ambient temperature (23 C) and irradiated with blue LEDs (30 W, Xmax = 450 nm) which was placed 20.0 m from the vial for 12 h. To determine the yield of the products, an internal standard, trifluorotoluene (PhCF3) (14.6 mg, 12.3 pL, 0.100 mmol, 0.500 equiv) was added to the vial. Then, a 100 pL of the reaction mixture was taken and then dilute with 500 pL CD3CN followed by 19F NMR (the NMR sample was recombined with the rest of the reaction mixture afterward) . The combined reaction mixture was then purified by HPLC on the Luna PFP(2) preparative column (250 x 21.2 mm) column eluting with MeCN:H20 (v/v) with a flow rate of 10.6 mL/min to provide the purified products. In cases of closely-eluting peaks, products were isolated as a mixture of isomers. Afterwards, the products were extracted with CDC13 (3 x 1 mL) , dried with magnesium sulfate, and filtered. The filtrate was concentrated in vacuo to afford the desired product (s). For very volatile compounds, the products were extracted immediately with CDCI3 (l x l mL) and then directly characterized. 1H and 13C NMR of these Compound (s) contains MeCN residue signal (1H NMR: □ 1.94, 13C NMR: u 118.26, 1.32 in CDCI3 )
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