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[ CAS No. 71942-14-8 ] {[proInfo.proName]}

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Chemical Structure| 71942-14-8
Chemical Structure| 71942-14-8
Structure of 71942-14-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 71942-14-8 ]

CAS No. :71942-14-8 MDL No. :MFCD12405395
Formula : C8H9BrO Boiling Point : No data available
Linear Structure Formula :- InChI Key :GJVYZGLNIKGKTE-UHFFFAOYSA-N
M.W : 201.06 Pubchem ID :12617738
Synonyms :

Calculated chemistry of [ 71942-14-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.1
TPSA : 20.23 ?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) : -5.4 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.06
Log Po/w (XLOGP3) : 2.99
Log Po/w (WLOGP) : 2.77
Log Po/w (MLOGP) : 2.88
Log Po/w (SILICOS-IT) : 2.94
Consensus Log Po/w : 2.73

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.41
Solubility : 0.0775 mg/ml ; 0.000385 mol/l
Class : Soluble
Log S (Ali) : -3.08
Solubility : 0.168 mg/ml ; 0.000834 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.45
Solubility : 0.0707 mg/ml ; 0.000352 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 71942-14-8 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H302 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 71942-14-8 ]

* 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 [ 71942-14-8 ]

[ 71942-14-8 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 576-23-8 ]
  • [ 71942-14-8 ]
YieldReaction ConditionsOperation in experiment
22% With (η5-indenyl)(η4-1,5-cyclooctadiene)iridium(I); 1,2-bis-(diphenylphosphino)ethane; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In cyclohexane at 100℃; for 50 h; Sealed tube In a sealed tube DPPE (0.431 g, 1.08 mmol), 4,4,5, 5-tetramethyl-l,3,2-dioxaborolane (1.73 g, 13.5 mmol), (l,5-Cyclooctadiene)-eta5- indenyl)iridium(I) (0.449 g, 1.08 mmol) and l-bromo-2,3-dimethylbenzene (1.00 g, 5.40 mmol) were placed in cyclohexane (6 mL) and was heated to 100°C for 50hr. The reaction was concentrated down and brought up in acetone (5 mL) and oxzone (3.32 g, 5.40 mmol) was added and stirred for 10 min. The reaction was quenched with saturated NaHS03 and was extracted with DCM (3x20 ml). The extracts were washed with brine, water and concentrated. The residue was passed through a plug of silica eluting with DCM to provide 3-bromo-4,5- dimethylphenol (238 mg, 1.18 mmol, 22 percent yield).
Reference: [1] Patent: WO2017/201161, 2017, A1, . Location in patent: Paragraph 0830
[2] Journal of the American Chemical Society, 2003, vol. 125, # 26, p. 7792 - 7793
  • 2
  • [ 95-65-8 ]
  • [ 71942-14-8 ]
Reference: [1] Journal of the Chemical Society, Chemical Communications, 1980, # 3, p. 110 - 111
  • 3
  • [ 22802-39-7 ]
  • [ 71942-14-8 ]
Reference: [1] Tetrahedron Letters, 1982, vol. 23, # 16, p. 1673 - 1676
[2] Tetrahedron Letters, 1982, vol. 23, # 16, p. 1673 - 1676
  • 4
  • [ 126-81-8 ]
  • [ 71942-14-8 ]
  • [ 203808-81-5 ]
Reference: [1] Journal of the Chemical Society, 1913, vol. 103, p. 2181
[2] Journal of the Chemical Society, 1913, vol. 103, p. 1301
[3] Proceedings of the Chemical Society, London, 1913, vol. 28, p. 333[4] Journal of the Chemical Society, 1913, vol. 103, p. 989
  • 5
  • [ 42824-00-0 ]
  • [ 71942-14-8 ]
  • [ 203808-81-5 ]
Reference: [1] Journal fur Praktische Chemie - Chemiker - Zeitung, 1998, vol. 340, # 2, p. 175 - 177
  • 6
  • [ 95-65-8 ]
  • [ 22802-39-7 ]
  • [ 71942-14-8 ]
  • [ 71942-13-7 ]
  • [ 22802-40-0 ]
Reference: [1] Canadian Journal of Chemistry, 1983, vol. 61, p. 1045 - 1052
  • 7
  • [ 408314-23-8 ]
  • [ 71942-14-8 ]
  • [ 203808-81-5 ]
Reference: [1] Journal of the Chemical Society, 1914, vol. 105, p. 166
[2] Journal of the Chemical Society, 1913, vol. 103, p. 2181
[3] Journal of the Chemical Society, 1914, vol. 105, p. 166
  • 8
  • [ 7789-69-7 ]
  • [ 126-81-8 ]
  • [ 71942-14-8 ]
  • [ 203808-81-5 ]
  • [ 838841-06-8 ]
Reference: [1] Journal of the Chemical Society, 1913, vol. 103, p. 2181
[2] Journal of the Chemical Society, 1913, vol. 103, p. 1301
[3] Proceedings of the Chemical Society, London, 1913, vol. 28, p. 333[4] Journal of the Chemical Society, 1913, vol. 103, p. 989
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