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[ CAS No. 17623-96-0 ] {[proInfo.proName]}

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Chemical Structure| 17623-96-0
Chemical Structure| 17623-96-0
Structure of 17623-96-0 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 17623-96-0 ]

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Product Details of [ 17623-96-0 ]

CAS No. :17623-96-0 MDL No. :MFCD07784485
Formula : C9H9Br Boiling Point : No data available
Linear Structure Formula :- InChI Key :APYDCTAPNKFTRB-UHFFFAOYSA-N
M.W : 197.07 Pubchem ID :10965463
Synonyms :

Calculated chemistry of [ 17623-96-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.33
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.94
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
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) : -5.34 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.24
Log Po/w (XLOGP3) : 3.04
Log Po/w (WLOGP) : 2.55
Log Po/w (MLOGP) : 3.32
Log Po/w (SILICOS-IT) : 3.39
Consensus Log Po/w : 2.91

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -3.42
Solubility : 0.0747 mg/ml ; 0.000379 mol/l
Class : Soluble
Log S (Ali) : -2.71
Solubility : 0.388 mg/ml ; 0.00197 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.85
Solubility : 0.0276 mg/ml ; 0.00014 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.23

Safety of [ 17623-96-0 ]

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

Application In Synthesis of [ 17623-96-0 ]

* 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 [ 17623-96-0 ]

[ 17623-96-0 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 1775-27-5 ]
  • [ 17623-96-0 ]
YieldReaction ConditionsOperation in experiment
90% at 20℃; for 24 h; In a 250 ml dry three-necked flask, 22.0 g of bromo compound I, 0.67 g of 5percent palladium on carbon,Add ethanol 250ml, into the hydrogen, the reaction pressure control at 2.5MPa,Bromide compound I and hydrogen molar ratio of 1:50, room temperature stirring reaction 24h,The palladium carbon was recovered by filtration and the solvent was evaporated. To give 18.5 g of the oily compound II as an oil. Yield 90percent.
Reference: [1] Patent: CN104945265, 2017, B, . Location in patent: Paragraph 0036; 0037; 0038
  • 2
  • [ 4254-29-9 ]
  • [ 17623-96-0 ]
Reference: [1] Journal of Medicinal Chemistry, 1994, vol. 37, # 11, p. 1586 - 1601
[2] Tetrahedron Letters, 2009, vol. 50, # 52, p. 7314 - 7317
[3] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 11, p. 1453 - 1461
[4] Journal of Medicinal Chemistry, 1968, vol. 11, p. 402 - 403
[5] Patent: EP1586561, 2005, A1, . Location in patent: Page/Page column 25
[6] Patent: WO2017/214505, 2017, A1, . Location in patent: Paragraph 000954; 000955
  • 3
  • [ 4254-29-9 ]
  • [ 7789-60-8 ]
  • [ 17623-96-0 ]
Reference: [1] Patent: US4500713, 1985, A,
  • 4
  • [ 496-11-7 ]
  • [ 17623-96-0 ]
  • [ 24373-98-6 ]
Reference: [1] Tetrahedron, 1989, vol. 45, # 24, p. 7869 - 7878
  • 5
  • [ 4254-31-3 ]
  • [ 17623-96-0 ]
Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 11, p. 1453 - 1461
  • 6
  • [ 615-13-4 ]
  • [ 17623-96-0 ]
Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 11, p. 1453 - 1461
  • 7
  • [ 83-33-0 ]
  • [ 17623-96-0 ]
Reference: [1] Patent: CN104945265, 2017, B,
  • 8
  • [ 95-13-6 ]
  • [ 17623-96-0 ]
Reference: [1] Russian Chemical Bulletin, 1993, vol. 42, # 9, p. 1573 - 1578[2] Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1993, # 9, p. 1637 - 1642
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