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[ CAS No. 2416-95-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2416-95-7
Chemical Structure| 2416-95-7
Structure of 2416-95-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2416-95-7 ]

CAS No. :2416-95-7 MDL No. :MFCD20257818
Formula : C24H34O2 Boiling Point : -
Linear Structure Formula :- InChI Key :QAISRHCMPQROAX-UHFFFAOYSA-N
M.W : 354.53 Pubchem ID :11602828
Synonyms :
Chemical Name :3,3',5,5'-Tetraisopropylbiphenyl-4,4'-diol

Calculated chemistry of [ 2416-95-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 26
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.5
Num. rotatable bonds : 5
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 114.24
TPSA : 40.46 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : No
P-gp substrate : Yes
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -3.25 cm/s

Lipophilicity

Log Po/w (iLOGP) : 4.36
Log Po/w (XLOGP3) : 7.34
Log Po/w (WLOGP) : 7.26
Log Po/w (MLOGP) : 5.26
Log Po/w (SILICOS-IT) : 6.99
Consensus Log Po/w : 6.24

Druglikeness

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

Water Solubility

Log S (ESOL) : -6.67
Solubility : 0.0000751 mg/ml ; 0.000000212 mol/l
Class : Poorly soluble
Log S (Ali) : -8.02
Solubility : 0.0000034 mg/ml ; 0.0000000096 mol/l
Class : Poorly soluble
Log S (SILICOS-IT) : -7.01
Solubility : 0.0000343 mg/ml ; 0.0000000968 mol/l
Class : Poorly soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.72

Safety of [ 2416-95-7 ]

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 [ 2416-95-7 ]

* 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 [ 2416-95-7 ]

[ 2416-95-7 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 2078-54-8 ]
  • [ 2416-95-7 ]
Reference: [1] Catalysis Science and Technology, 2017, vol. 7, # 15, p. 3205 - 3209
[2] Chemical and Pharmaceutical Bulletin, 2005, vol. 53, # 3, p. 344 - 346
[3] Biological and Pharmaceutical Bulletin, 2005, vol. 28, # 6, p. 1120 - 1122
[4] Journal of the American Chemical Society, 2014, vol. 136, # 19, p. 6782 - 6785
[5] Organic Process Research and Development, 2014, vol. 18, # 1, p. 152 - 156
[6] Chemistry Letters, 1995, # 9, p. 845 - 846
[7] Chemistry - A European Journal, 2019,
[8] Patent: US2018/185299, 2018, A1,
  • 2
  • [ 2178-51-0 ]
  • [ 2416-95-7 ]
Reference: [1] Journal of the American Chemical Society, 1957, vol. 79, p. 5019,5021
[2] Synthesis, 1978, p. 165 - 204
[3] Journal of Organic Chemistry, 1971, vol. 36, # 10, p. 1339 - 1341
[4] Biological and Pharmaceutical Bulletin, 2007, vol. 30, # 8, p. 1565 - 1568
[5] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 8, p. 3207 - 3211
  • 3
  • [ 2078-54-8 ]
  • [ 2178-51-0 ]
  • [ 2416-95-7 ]
Reference: [1] Bulletin of the Chemical Society of Japan, 1992, vol. 65, # 2, p. 620 - 622
[2] Tetrahedron Letters, 1990, vol. 31, # 26, p. 3771 - 3774
  • 4
  • [ 2078-54-8 ]
  • [ 2178-51-0 ]
  • [ 2416-95-7 ]
  • [ 22944-23-6 ]
Reference: [1] Bulletin of the Chemical Society of Japan, 1992, vol. 65, # 2, p. 620 - 622
  • 5
  • [ 99-62-7 ]
  • [ 2416-95-7 ]
Reference: [1] Journal of the American Chemical Society, 2014, vol. 136, # 19, p. 6782 - 6785
  • 6
  • [ 99-96-7 ]
  • [ 2416-95-7 ]
Reference: [1] Organic Process Research and Development, 2014, vol. 18, # 1, p. 152 - 156
  • 7
  • [ 13423-73-9 ]
  • [ 2416-95-7 ]
Reference: [1] Organic Process Research and Development, 2014, vol. 18, # 1, p. 152 - 156
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