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[ CAS No. 35065-86-2 ] {[proInfo.proName]}

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Chemical Structure| 35065-86-2
Chemical Structure| 35065-86-2
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Product Details of [ 35065-86-2 ]

CAS No. :35065-86-2 MDL No. :MFCD08063242
Formula : C8H7BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :CDLTWXBTYNNYLN-UHFFFAOYSA-N
M.W : 215.04 Pubchem ID :141946
Synonyms :

Calculated chemistry of [ 35065-86-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 45.64
TPSA : 26.3 ?2

Pharmacokinetics

GI absorption : High
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) : -5.99 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.27
Log Po/w (XLOGP3) : 2.28
Log Po/w (WLOGP) : 2.37
Log Po/w (MLOGP) : 2.67
Log Po/w (SILICOS-IT) : 2.36
Consensus Log Po/w : 2.39

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.88
Solubility : 0.283 mg/ml ; 0.00131 mol/l
Class : Soluble
Log S (Ali) : -2.47
Solubility : 0.73 mg/ml ; 0.00339 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.33
Solubility : 0.0999 mg/ml ; 0.000465 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.69

Safety of [ 35065-86-2 ]

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 [ 35065-86-2 ]

* 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.

  • Upstream synthesis route of [ 35065-86-2 ]
  • Downstream synthetic route of [ 35065-86-2 ]

[ 35065-86-2 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 35065-86-2 ]
  • [ 61791-99-9 ]
Reference: [1] Taiwan Yaoxue Zazhi, 1952, vol. 4, p. 38[2] Journal of the Chemical Society, 1958, p. 146,149
  • 2
  • [ 35065-86-2 ]
  • [ 55736-69-1 ]
YieldReaction ConditionsOperation in experiment
99%
Stage #1: With aluminum (III) chloride In dichloromethane at 140 - 150℃; for 2 h;
Stage #2: With hydrogenchloride; water In dichloromethaneHeating / reflux
Intermediate 2; 1-(2-bromo-6-hydroxypherjy.)ethanone; The mixture of 3-Bromophenyl acetate (36.0 g, 167 mmol) and uohydrous AlCl3 (33.5 g 251 mmol) was heated to 140 - 150 0C for 2 h. To the resulting black solid was added 100 ml of 5percent HCI and the mixture was heated on boiling wafer bath until the solid material dissolved. After cooling to the room temperature the precipitated brown oil was extracted with CH2Cl2 (3 x 150 ml) and to the organic layer was added 300 ml of 5N NaOH. The formed precipitate was dissolved In water, organic layer was separated and the water one was acidified to pH ~ 2 and extracted with EfOAc (5 x 150 mL). Combined extracts were dried over Na2SO4 and evaporated to give the title compound as beige crystals (35.8 g, 99percent).GC/MS data: 214 (M)+ (Calculated for C8H7BrO2 215.05), (calc. monoisαtopic mass is (M)* 213.96). 1H NMR data (DMSO-d6): 11.97 (s, 1H, OH), 7.78 (d, 1H, J=8.3 Hz, Ar-H), 7.19 (d, 1H, J=2.0 Hz, Ar-H), 7.13 (dd, 1H, J,=8.3 Hz1 J2=ZO Hz1 Ar-H), 2.60 (s, 3H, CH3).
Reference: [1] Patent: WO2007/88450, 2007, A2, . Location in patent: Page/Page column 21
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