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[ CAS No. 345965-52-8 ] {[proInfo.proName]}

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Chemical Structure| 345965-52-8
Chemical Structure| 345965-52-8
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Product Details of [ 345965-52-8 ]

CAS No. :345965-52-8 MDL No. :MFCD07374439
Formula : C10H9BrO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :BYJIXWOWTNEVFO-UHFFFAOYSA-N
M.W : 241.08 Pubchem ID :16227966
Synonyms :

Calculated chemistry of [ 345965-52-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 53.07
TPSA : 37.3 ?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) : -6.05 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.02
Log Po/w (XLOGP3) : 2.42
Log Po/w (WLOGP) : 2.5
Log Po/w (MLOGP) : 2.59
Log Po/w (SILICOS-IT) : 2.9
Consensus Log Po/w : 2.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.07
Solubility : 0.206 mg/ml ; 0.000853 mol/l
Class : Soluble
Log S (Ali) : -2.85
Solubility : 0.344 mg/ml ; 0.00143 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.45
Solubility : 0.0859 mg/ml ; 0.000356 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.44

Safety of [ 345965-52-8 ]

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 [ 345965-52-8 ]

* 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.

  • Upstream synthesis route of [ 345965-52-8 ]
  • Downstream synthetic route of [ 345965-52-8 ]

[ 345965-52-8 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 345965-52-8 ]
  • [ 1014645-87-4 ]
Reference: [1] Patent: WO2012/76063, 2012, A1,
  • 2
  • [ 345965-52-8 ]
  • [ 1215205-50-7 ]
YieldReaction ConditionsOperation in experiment
80% With thionyl chloride In methanol at 0 - 70℃; To a 50 mL round-bottom flask was added l-(4-bromophenyl)cyclopropane-1- carboxylic acid 149a (2 g, 8.30 mmol, 1.00 equiv.) and methanol (20 mL). Thionyl chloride(2.96 g, 24.88 mmol, 3.00 equiv.) was added drop·wise with stirring at 0°C. The resultingmixture was stined at 70 °C ovemight. After cooling to room temperature, the reaction wasquenched by the addition of water/ice. The aqueous mixture was extracted with ethyl acetate5 (50 mL x 2). The combined organic extracts were vvashed with brine (50 rnL x 2, dried overanhydrous sodium sulfate, and concentrated under vacuum. The crude product was purifiedby Flash-Prep-HPLC eluting with EA/PE (from 0percent to 10percent '.vithin 20 rnin) to give methyl1-(4-bromophenyl)cyclopropa.ne-l-carboxyate 149b (l.7g, 80percent;) as colorless oil
Reference: [1] Patent: WO2018/39386, 2018, A1, . Location in patent: Page/Page column 295; 296
  • 3
  • [ 345965-52-8 ]
  • [ 64-17-5 ]
  • [ 1215205-50-7 ]
Reference: [1] Organic Process Research and Development, 2017, vol. 21, # 11, p. 1859 - 1863
[2] Patent: WO2010/141761, 2010, A2, . Location in patent: Page/Page column 47
[3] Patent: US2011/82164, 2011, A1, . Location in patent: Page/Page column 24
[4] Patent: US2011/82181, 2011, A1, . Location in patent: Page/Page column 16
[5] Patent: WO2012/78593, 2012, A2, . Location in patent: Page/Page column 124
[6] Patent: WO2012/78805, 2012, A1, . Location in patent: Page/Page column 92
[7] Patent: US2012/258987, 2012, A1, . Location in patent: Page/Page column 42
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