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[ CAS No. 232275-51-3 ] {[proInfo.proName]}

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Chemical Structure| 232275-51-3
Chemical Structure| 232275-51-3
Structure of 232275-51-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 232275-51-3 ]

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Product Details of [ 232275-51-3 ]

CAS No. :232275-51-3 MDL No. :MFCD11227148
Formula : C7H3BrCl2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SSWALODYSQLVPK-UHFFFAOYSA-N
M.W : 269.91 Pubchem ID :22571822
Synonyms :

Calculated chemistry of [ 232275-51-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.12
TPSA : 37.3 ?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) : -5.53 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.75
Log Po/w (XLOGP3) : 3.4
Log Po/w (WLOGP) : 3.45
Log Po/w (MLOGP) : 3.5
Log Po/w (SILICOS-IT) : 3.19
Consensus Log Po/w : 3.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.96
Solubility : 0.0296 mg/ml ; 0.00011 mol/l
Class : Soluble
Log S (Ali) : -3.86
Solubility : 0.037 mg/ml ; 0.000137 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.86
Solubility : 0.0376 mg/ml ; 0.000139 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.55

Safety of [ 232275-51-3 ]

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

Application In Synthesis of [ 232275-51-3 ]

* 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 [ 232275-51-3 ]

[ 232275-51-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 232275-53-5 ]
  • [ 232275-51-3 ]
  • 2
  • [ 232275-51-3 ]
  • [ 74-88-4 ]
  • [ 232275-53-5 ]
YieldReaction ConditionsOperation in experiment
98.10% With potassium carbonate; In acetonitrile; at 20℃; for 16.0h; General procedure: To a 100 mL 1-neck round bottom flask, the mixture of 4-bromo-2,6-dichloro-benzoic acid (500 mg, 1.85 mmol), iodomethane (788.82 mg, 5.56 mmol, 345.97 uL), Potassium carbonate (1.28 g, 9.26 mmol, 559.01 uL) in acetonitrile (20 mL) was stirred at RT for 6 h, then it was diluted with water, extracted with EA, dried with Na2SO4, concentrated to afford methyl 4-bromo-2,6-dichloro-benzoate (516 mg, 1.82 mmol, 98.10% yield) as yellow oil, it was used to next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.51 (s, 2H), 3.97 (s, 3H).
95.06% With potassium carbonate; In N,N-dimethyl-formamide; at 20℃; To a solution of 0190-1 (2.00 g, 7.41 mmol) and CI (1.05 g, 7.41 mmol) in DMF (5 mL), was added K2CO3 (1.54 g, 11.11 mmol) and the mixture was stirred at room temperature for overnight. After the reaction was finished, water was added and the mixture was filtered and the liquid layer was extracted with EA (20 mL x 3), the organic phase was combined and washed with water then brine, dried over Na2SC>4, concentrated and purified by prep-HPLC to get 0190-2 (2.0 g, 95.06% yield) as a white solid. Agilent LCMS 1200-6120, Column: Halo Cl 8 (30 mm*4.6 mm*2.7 pm); Column Temperature: 40 C; Flow Rate: 3.0 mL/min; Mobile Phase: from 95% [water + 10 mM TFA] and 5% [CH3CN] to 0% [water + 10 mM TFA] and 100% [CH3CN] in 0.8 min, then under this condition for 0.4 min, finally changed to 95% [water + 10 mM TFA] and 5% [CH3CN] in 0.01 min. Purity is 93.35%. Rt = 0.853 min; MS Calcd.:282.7; MS Found: 283.7 [M+H]+.
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