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[ CAS No. 51417-51-7 ] {[proInfo.proName]}

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Chemical Structure| 51417-51-7
Chemical Structure| 51417-51-7
Structure of 51417-51-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 51417-51-7 ]

CAS No. :51417-51-7 MDL No. :MFCD00799492
Formula : C8H6BrN Boiling Point : -
Linear Structure Formula :- InChI Key :RDSVSEFWZUWZHW-UHFFFAOYSA-N
M.W : 196.04 Pubchem ID :2757020
Synonyms :
Chemical Name :7-Bromoindole

Calculated chemistry of [ 51417-51-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 0.0
Num. H-bond donors : 1.0
Molar Refractivity : 46.0
TPSA : 15.79 ?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) : -5.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 2.74
Log Po/w (WLOGP) : 2.93
Log Po/w (MLOGP) : 2.31
Log Po/w (SILICOS-IT) : 3.25
Consensus Log Po/w : 2.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.45
Solubility : 0.0699 mg/ml ; 0.000357 mol/l
Class : Soluble
Log S (Ali) : -2.73
Solubility : 0.368 mg/ml ; 0.00188 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.14
Solubility : 0.0142 mg/ml ; 0.0000726 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.31

Safety of [ 51417-51-7 ]

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

Application In Synthesis of [ 51417-51-7 ]

* 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 [ 51417-51-7 ]
  • Downstream synthetic route of [ 51417-51-7 ]

[ 51417-51-7 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 51417-51-7 ]
  • [ 73183-34-3 ]
  • [ 642494-37-9 ]
YieldReaction ConditionsOperation in experiment
25 g With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate In dimethyl sulfoxide at 85℃; for 2 h; 7-bromoindole (20 g, 0.102mol) was dissolved in DMSO (100mL) in an 1 L single neck flask, and bis(pinacolato)diboron (39 g, 0.153 mol), [1,1’-bis(diphenylphosphino)ferrocene]dichloropalladium (Pd(dppf)Cl2, 4 g, 0.005 mol),and potassium acetate (15 g, 0.153 mol) were added. The system was heated to 85 °C to react for 2 h. Water was addedto quench the reaction. The mixture was extracted with ethyl acetate for 3 times, dried over sodium sulfate, concentrated,and subjected to column chromatography to obtain the product (25 g, 0.103 mol). 1H NMR (400 MHz, CDCl3): δ 9.29(s, 1H), 7.82 (d, J = 7.9 Hz, 1H), 7.70 (d, J = 7.0 Hz, 1H), 7.32-7.29 (m, 1H), 7.21-7.14 (m, 1H), 6.62-6.57 (m, 1H), 1.44(s, 12H). MS (ESI) (m/z): [M+H]+ 244.1.
Reference: [1] Synlett, 2003, # 8, p. 1204 - 1206
[2] Advanced Synthesis and Catalysis, 2017, vol. 359, # 19, p. 3421 - 3427
[3] Journal of the American Chemical Society, 2017, vol. 139, # 24, p. 8267 - 8276
[4] European Journal of Organic Chemistry, 2016, vol. 2016, # 27, p. 4621 - 4628
[5] Patent: JP2015/528445, 2015, A, . Location in patent: Paragraph 0047; 0065
[6] Patent: EP3345906, 2018, A1, . Location in patent: Paragraph 0332; 0333
  • 2
  • [ 51417-51-7 ]
  • [ 25015-63-8 ]
  • [ 642494-37-9 ]
Reference: [1] Journal of Organic Chemistry, 2006, vol. 71, # 15, p. 5807 - 5810
[2] Patent: WO2006/10142, 2006, A2, . Location in patent: Page/Page column 83; 84
  • 3
  • [ 51417-51-7 ]
  • [ 642494-37-9 ]
Reference: [1] Heterocycles, 2010, vol. 80, # 2, p. 1267 - 1274
[2] Patent: US2015/318483, 2015, A1,
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