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[ CAS No. 190723-12-7 ] {[proInfo.proName]}

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Chemical Structure| 190723-12-7
Chemical Structure| 190723-12-7
Structure of 190723-12-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 190723-12-7 ]

CAS No. :190723-12-7 MDL No. :MFCD08695787
Formula : C6H2Br2O4S Boiling Point : No data available
Linear Structure Formula :- InChI Key :ZZYYIZHQMCEKLG-UHFFFAOYSA-N
M.W : 329.95 Pubchem ID :16640107
Synonyms :

Calculated chemistry of [ 190723-12-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 53.64
TPSA : 102.84 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : 2.7
Log Po/w (WLOGP) : 2.67
Log Po/w (MLOGP) : 1.7
Log Po/w (SILICOS-IT) : 2.76
Consensus Log Po/w : 2.18

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.74
Solubility : 0.0601 mg/ml ; 0.000182 mol/l
Class : Soluble
Log S (Ali) : -4.51
Solubility : 0.0101 mg/ml ; 0.0000307 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -2.09
Solubility : 2.67 mg/ml ; 0.00809 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.72

Safety of [ 190723-12-7 ]

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

Application In Synthesis of [ 190723-12-7 ]

* 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 [ 190723-12-7 ]

[ 190723-12-7 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 108-24-7 ]
  • [ 190723-12-7 ]
  • [ 1015423-45-6 ]
YieldReaction ConditionsOperation in experiment
at 140℃; for 12h;Inert atmosphere; Acetic anhydride (7.6 mL) was added to 1 (0.50 g, 1.52 mmol) under a nitrogen atmosphere. The mixture was heated to 140 C for 12 h and then cooled to room temperature. The volatile compounds were removed in vacuo and the crude product was used in the next step without purification. After the brown solid was dissolved in toluene (1 mL), 4-trifluoromethylaniline (294 mg, 1.83 mmol) was added to the solution and the mixture was heated under reflux for 24 h. After removing the volatile components, thionyl chloride was added to the residue and the reaction mixture was stirred at 90 C for 12 h. The volatile components were removed in vacuo and the residue was extracted with chloroform. The organic phase was dried with anhydrous sodium sulfate and the solvent was removed under a reduced pressure. The crude product was purified by column chromatography with silica gel using chloroform as the eluent. The product was recrystallized from ethanol to afford TPD1 as an off-white solid with a yield of 81%. 1H NMR (500 MHz, CDCl3, rt): δ 7.76 (d, J = 8.0 Hz, 2H), 7.55 (d, J = 8.0 Hz, 2H). 13C NMR (125 MHz, CDCl3, rt): δ 158.73, 134.55, 133.86, 130.14, 126.42, 126.26, 126.23, 114.90. Anal. Calcd for C13H4Br2F3NO2S: C, 34.31; H, 0.89; N, 3.08. Found: C, 34.11; H, 0.95; N, 3.06.
  • 3
  • [ 190723-12-7 ]
  • [ 1231160-83-0 ]
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