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[ CAS No. 4783-86-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 4783-86-2
Chemical Structure| 4783-86-2
Structure of 4783-86-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 4783-86-2 ]

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Product Details of [ 4783-86-2 ]

CAS No. :4783-86-2 MDL No. :MFCD00235157
Formula : C11H9NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :OATKXQIGHQXTDO-UHFFFAOYSA-N
M.W : 171.20 Pubchem ID :249651
Synonyms :

Calculated chemistry of [ 4783-86-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 50.75
TPSA : 22.12 ?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) : -5.65 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.16
Log Po/w (XLOGP3) : 2.38
Log Po/w (WLOGP) : 2.87
Log Po/w (MLOGP) : 1.74
Log Po/w (SILICOS-IT) : 2.56
Consensus Log Po/w : 2.34

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.95
Solubility : 0.191 mg/ml ; 0.00112 mol/l
Class : Soluble
Log S (Ali) : -2.49
Solubility : 0.56 mg/ml ; 0.00327 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.28
Solubility : 0.00905 mg/ml ; 0.0000528 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.43

Safety of [ 4783-86-2 ]

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

Application In Synthesis of [ 4783-86-2 ]

* 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 [ 4783-86-2 ]
  • Downstream synthetic route of [ 4783-86-2 ]

[ 4783-86-2 ] Synthesis Path-Upstream   1~18

  • 1
  • [ 7379-35-3 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Tetrahedron Letters, 2006, vol. 47, # 29, p. 5045 - 5048
[2] Patent: US6500948, 2002, B1,
[3] Patent: US6153757, 2000, A,
[4] Patent: US6750228, 2004, B1,
[5] Tetrahedron Letters, 2010, vol. 51, # 2, p. 248 - 251
[6] Patent: US2010/174089, 2010, A1, . Location in patent: Page/Page column 4
  • 2
  • [ 15854-87-2 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Catalysis Science and Technology, 2016, vol. 6, # 6, p. 1701 - 1709
[2] Synlett, 2012, # 1, p. 101 - 106
[3] Tetrahedron Letters, 2006, vol. 47, # 29, p. 5045 - 5048
  • 3
  • [ 626-61-9 ]
  • [ 100-67-4 ]
  • [ 4783-86-2 ]
Reference: [1] Chemistry - A European Journal, 2012, vol. 18, # 6, p. 1800 - 1810
[2] Chemistry of Heterocyclic Compounds (New York, NY, United States), 1988, p. 290 - 294[3] Khimiya Geterotsiklicheskikh Soedinenii, 1988, vol. 24, # 3, p. 356 - 360
[4] Organic Process Research and Development, 2010, vol. 14, # 3, p. 644 - 649
  • 4
  • [ 1120-87-2 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Chemical Communications, 2013, vol. 49, # 68, p. 7483 - 7485
[2] Tetrahedron Letters, 2006, vol. 47, # 29, p. 5045 - 5048
  • 5
  • [ 626-61-9 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Chemical Communications, 2013, vol. 49, # 68, p. 7483 - 7485
  • 6
  • [ 626-64-2 ]
  • [ 4783-86-2 ]
Reference: [1] Chemical Science, 2015, vol. 6, # 2, p. 1277 - 1281
  • 7
  • [ 626-64-2 ]
  • [ 24388-23-6 ]
  • [ 4783-86-2 ]
Reference: [1] Journal of the American Chemical Society, 2017, vol. 139, # 13, p. 4769 - 4779
  • 8
  • [ 15854-87-2 ]
  • [ 139-02-6 ]
  • [ 4783-86-2 ]
Reference: [1] Tetrahedron, 2002, vol. 58, # 24, p. 4931 - 4935
  • 9
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Angewandte Chemie - International Edition, 2018, vol. 57, # 34, p. 11035 - 11039[2] Angew. Chem., 2018, vol. 130, # 34, p. 11201 - 11205,5
  • 10
  • [ 626-61-9 ]
  • [ 139-02-6 ]
  • [ 4783-86-2 ]
Reference: [1] Chemische Berichte, 1915, vol. 48, p. 961
  • 11
  • [ 139-02-6 ]
  • [ 5421-92-1 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Journal of the American Chemical Society, 1937, vol. 59, p. 297,299
[2] DRP/DRBP Org.Chem., [3] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 19, p. 1120
  • 12
  • [ 163632-01-7 ]
  • [ 4783-86-2 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 3, p. 283 - 291
[2] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 3, p. 283 - 291
  • 13
  • [ 504-24-5 ]
  • [ 4783-86-2 ]
Reference: [1] Angewandte Chemie - International Edition, 2018, vol. 57, # 34, p. 11035 - 11039[2] Angew. Chem., 2018, vol. 130, # 34, p. 11201 - 11205,5
  • 14
  • [ 75-05-8 ]
  • [ 163632-01-7 ]
  • [ 4783-86-2 ]
Reference: [1] Bioorganic and Medicinal Chemistry, 1998, vol. 6, # 3, p. 283 - 291
  • 15
  • [ 5421-92-1 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Chemische Berichte, 1956, vol. 89, p. 2921,2928
[2] DRP/DRBP Org.Chem., [3] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 19, p. 1120
  • 16
  • [ 100-67-4 ]
  • [ 5421-92-1 ]
  • [ 108-95-2 ]
  • [ 4783-86-2 ]
Reference: [1] Chemische Berichte, 1941, vol. 64, p. 1049,1056
  • 17
  • [ 4783-86-2 ]
  • [ 6091-44-7 ]
  • [ 2767-90-0 ]
Reference: [1] Chemische Berichte, 1958, vol. 91, p. 1266,1272
  • 18
  • [ 4783-86-2 ]
  • [ 142-95-0 ]
  • [ 64690-19-3 ]
Reference: [1] Doklady Chemistry, 1984, vol. 275, p. 97 - 100[2] Doklady Akademii Nauk SSSR, 1984, vol. 275, p. 385 - 387
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