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[ CAS No. 39149-80-9 ] {[proInfo.proName]}

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Chemical Structure| 39149-80-9
Chemical Structure| 39149-80-9
Structure of 39149-80-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 39149-80-9 ]

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Product Details of [ 39149-80-9 ]

CAS No. :39149-80-9 MDL No. :MFCD00043897
Formula : C7H13BrO2 Boiling Point : -
Linear Structure Formula :- InChI Key :CVAWKJKISIPBOD-UHFFFAOYSA-N
M.W : 209.08 Pubchem ID :545327
Synonyms :

Calculated chemistry of [ 39149-80-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.86
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 44.96
TPSA : 26.3 ?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) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.47
Log Po/w (XLOGP3) : 2.29
Log Po/w (WLOGP) : 2.11
Log Po/w (MLOGP) : 2.12
Log Po/w (SILICOS-IT) : 1.64
Consensus Log Po/w : 2.13

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.38
Solubility : 0.87 mg/ml ; 0.00416 mol/l
Class : Soluble
Log S (Ali) : -2.48
Solubility : 0.693 mg/ml ; 0.00331 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.07
Solubility : 1.76 mg/ml ; 0.00843 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.29

Safety of [ 39149-80-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 39149-80-9 ]

* 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 [ 39149-80-9 ]

[ 39149-80-9 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 64-65-3 ]
  • [ 39149-80-9 ]
  • [ 129224-48-2 ]
  • 2
  • [ 39149-80-9 ]
  • [ 2051-99-2 ]
  • (S)-tert-butyl 2-(4-isobutylphenyl)propanoate [ No CAS ]
  • C17H26O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
General procedure: To a 50-mL two-neck round-bottom flask equipped with a cannula were added magnesium turnings (608 mg, 25 mmol), and the flask was heated at 80 C in vacuo for 1 h. A solution of the <strong>[2051-99-2]4-isobutylphenyl bromide</strong> (426 mg, 2.0 mmol) in THF (5 mL) was added dropwise over 3 min under argon. The mixture was heated at 50 C until the reaction was initiated. Additional <strong>[2051-99-2]4-isobutylphenyl bromide</strong> (1.71 g, 8.0 mmol) in THF (11.6 mL) was then added slowly via cannula over 15 min. The reaction mixture was heated at reflux for 3 h, after which a solution of 4-isobutylphenyl magnesium bromide 5 was obtained. To a separate 50-mL Schlenk tube was added anhydrous CoBr2 (21.9mg, 0.10mmol), and the tube was heated at 50C in vacuo for 2h. After cooling to room temperature, the cyclopropane-based bisoxazoline ligand 2 (0.12mmol) in THF (3mL) was added under argon. The resulting mixture was stirred for 1h at the same temperature, with 2-bromopropanoate 6 (1mmol) being added via syringe. The mixture solution was cooled to -80C, and the prepared Grignard reagent 5 (2.8mL, 0.5M in THF, 1.4mmol) was then added over 1h via syringe. The reaction mixture was stirred for another 6h at -80C and then quenched with saturated NH4Cl solution (5mL). The aqueous phase was extracted with diethyl ether (4×10mL). The combined organic phases were dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (n-hexane/ethyl acetate 100:1). 4.4.4 (S)-tert-Butyl 2-(4-isobutylphenyl)propanoate 7d Colorless oil, 84% yield, 78:22 er. The enantiomeric ratio was determined by HPLC with a Daicel Chiralcel OJ-H column (0.3% 2-propanol in n-hexane, 0.5 mL/min, 220 nm, minor tr = 8.76 min (R), major tr = 11.17 min (S)). [alpha]D20 = +5.5 (c 1.2, CHCl3). 1H NMR (300 MHz, CDCl3) delta: 7.20-7.17 (m, 2H), 7.07 (d, J = 8.2 Hz, 2H), 3.58 (q, J = 7.2 Hz, 1H), 2.44 (d, J = 7.2 Hz, 2H), 1.89-1.80 (m, 1H), 1.43 (d, J = 7.2 Hz, 3H), 1.39 (s, 9H), 0.89 (d, J = 6.6 Hz, 6H). 13C NMR (75 MHz, CDCl3) delta: 174.0, 140.1, 138.3, 129.1, 127.0, 80.2, 46.1, 45.0, 30.1, 27.9, 22.3, 18.4. HRMS (APCI-TOF): calcd for C17H25O2 [M-H]- 261.1855, found 261.1842.
  • 3
  • [ 39149-80-9 ]
  • [ 256652-04-7 ]
  • [ 1334591-50-2 ]
  • C17H20O2 [ No CAS ]
  • 4
  • [ 864772-18-9 ]
  • [ 39149-80-9 ]
  • C19H22O3 [ No CAS ]
  • C19H22O3 [ No CAS ]
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