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[ CAS No. 140632-12-8 ] {[proInfo.proName]}

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Chemical Structure| 140632-12-8
Chemical Structure| 140632-12-8
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Product Details of [ 140632-12-8 ]

CAS No. :140632-12-8 MDL No. :MFCD06761911
Formula : C8H10BrN Boiling Point : -
Linear Structure Formula :- InChI Key :DSAXBVQQKYZELF-LURJTMIESA-N
M.W : 200.08 Pubchem ID :2530257
Synonyms :

Calculated chemistry of [ 140632-12-8 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.62
TPSA : 26.02 Ų

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) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.1
Log Po/w (XLOGP3) : 1.87
Log Po/w (WLOGP) : 2.14
Log Po/w (MLOGP) : 2.61
Log Po/w (SILICOS-IT) : 2.27
Consensus Log Po/w : 2.2

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.64
Solubility : 0.462 mg/ml ; 0.00231 mol/l
Class : Soluble
Log S (Ali) : -2.04
Solubility : 1.83 mg/ml ; 0.00916 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.33
Solubility : 0.0934 mg/ml ; 0.000467 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 140632-12-8 ]

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

Application In Synthesis of [ 140632-12-8 ]

* 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 [ 140632-12-8 ]
  • Downstream synthetic route of [ 140632-12-8 ]

[ 140632-12-8 ] Synthesis Path-Upstream   1~10

  • 1
  • [ 2142-69-0 ]
  • [ 140632-12-8 ]
Reference: [1] Angewandte Chemie - International Edition, 2017, vol. 56, # 49, p. 15589 - 15593[2] Angew. Chem., 2017, vol. 129, p. 15795 - 15799,5
[3] Tetrahedron Asymmetry, 1996, vol. 7, # 10, p. 2809 - 2812
[4] Journal of Organic Chemistry, 2013, vol. 78, # 11, p. 5314 - 5327
[5] Organic Process Research and Development, 2014, vol. 18, # 6, p. 788 - 792
[6] Green Chemistry, 2017, vol. 19, # 2, p. 474 - 480
  • 2
  • [ 2142-69-0 ]
  • [ 109-73-9 ]
  • [ 140632-12-8 ]
  • [ 71-36-3 ]
Reference: [1] Catalysis Today, 2018, vol. 306, p. 96 - 101
  • 3
  • [ 943779-19-9 ]
  • [ 140632-12-8 ]
Reference: [1] Tetrahedron Asymmetry, 1996, vol. 7, # 10, p. 2809 - 2812
  • 4
  • [ 2142-69-0 ]
  • [ 140632-12-8 ]
Reference: [1] Organic and Biomolecular Chemistry, 2012, vol. 10, # 45, p. 8960 - 8962,3
[2] Organic and Biomolecular Chemistry, 2012, vol. 10, # 45, p. 8960 - 8962
  • 5
  • [ 2142-69-0 ]
  • [ 87227-77-8 ]
  • [ 109-97-7 ]
  • [ 140632-12-8 ]
Reference: [1] Advanced Synthesis and Catalysis, 2016, vol. 358, # 10, p. 1618 - 1624
  • 6
  • [ 2142-69-0 ]
  • [ 109-97-7 ]
  • [ 140632-12-8 ]
Reference: [1] Advanced Synthesis and Catalysis, 2016, vol. 358, # 10, p. 1618 - 1624
  • 7
  • [ 124-20-9 ]
  • [ 2142-69-0 ]
  • [ 57672-23-8 ]
  • [ 140632-12-8 ]
Reference: [1] Green Chemistry, 2017, vol. 19, # 2, p. 361 - 366
  • 8
  • [ 5411-56-3 ]
  • [ 140632-12-8 ]
Reference: [1] Tetrahedron Asymmetry, 1996, vol. 7, # 10, p. 2809 - 2812
  • 9
  • [ 1434602-33-1 ]
  • [ 140632-12-8 ]
Reference: [1] Journal of Organic Chemistry, 2013, vol. 78, # 11, p. 5314 - 5327
  • 10
  • [ 5411-56-3 ]
  • [ 140632-12-8 ]
Reference: [1] Green Chemistry, 2017, vol. 19, # 2, p. 474 - 480
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