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[ CAS No. 7254-19-5 ] {[proInfo.proName]}

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Chemical Structure| 7254-19-5
Chemical Structure| 7254-19-5
Structure of 7254-19-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 7254-19-5 ]

CAS No. :7254-19-5 MDL No. :MFCD00022705
Formula : C9H6BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :YAULOOYNCJDPPU-UHFFFAOYSA-N
M.W : 240.05 Pubchem ID :252137
Synonyms :

Calculated chemistry of [ 7254-19-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 52.96
TPSA : 53.09 ?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) : -5.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.5
Log Po/w (XLOGP3) : 3.0
Log Po/w (WLOGP) : 2.63
Log Po/w (MLOGP) : 1.8
Log Po/w (SILICOS-IT) : 2.54
Consensus Log Po/w : 2.29

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.66
Solubility : 0.052 mg/ml ; 0.000216 mol/l
Class : Soluble
Log S (Ali) : -3.78
Solubility : 0.0399 mg/ml ; 0.000166 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.52
Solubility : 0.0732 mg/ml ; 0.000305 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 7254-19-5 ]

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 [ 7254-19-5 ]

* 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.

  • Downstream synthetic route of [ 7254-19-5 ]

[ 7254-19-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7254-19-5 ]
  • [ 20358-03-6 ]
  • 5-bromo-N-(5-bromo-1,3-benzothiazol-2-yl)-1H-indole-2-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
2% With N-ethyl-N,N-diisopropylamine; HATU; In 1-methyl-pyrrolidin-2-one; at 20℃; for 48h; To a mixture of 5-bromo-1H-indole-2-carboxylic acid (264 mg, 1.10 mmol, 1.0 eq.) and HATU (500 mg, 1.32 mmol, 1.2 eq.) in NMP (30 mL) were added<strong>[20358-03-6]5-bromo-1,3-benzothiazol-2-amine</strong> (250 mg, 1.10 mmol, 1.0 eq.) andDIPEA (0.38 mL, 2.18 mmol, 2.0 eq.).The reaction mixture was stirred at room temperature during 48 hours, then quenched with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, the solvent evaporated under reduced pressure and the residue purified by silica gel flash-column chromatography (eluent: heptane/EtOAc, 90/10 to 70/30) to afford26das a pale green solid (8 mg, 2 percent).1H NMR(DMSO-d6, 400 MHz):d(ppm): 7.39 (1H, dd, J6-7= 8.8Hz, J6-4=1.4Hz, H6), 7.45 (1H, d, J7-6= 8.8Hz, H7), 7.29 (1H, t, J5-4=J5-6=7.6Hz, H5), 7.51 (1H, dd, J6?-7?= 8.8Hz, J6?-4?= 1.4Hz, H6?), 7.72 (1H, s, H3), 7.95 (1H, s, H4), 7.99 (1H, s, H4?), 8.01 (1H, d, J7?-6?= 8.8Hz, H7?), 12.21 (1H, s, indolic H), 13.17 (1H, s, amide H).13C NMR (DMSO-d6, 100 MHz):d(ppm): 106.5 (C3), 113.2 (C5), 115.1, 119.4 (C5?), 124.1 (C7?), 124.9, 126.7 (C6?), 127.9, 129.1 (C3a), 136.6 (C7a).HRMS calcd for C16H879Br81BrN3OS: m/z = 449.8734, found: 449.8657.
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