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[ CAS No. 98600-34-1 ] {[proInfo.proName]}

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Chemical Structure| 98600-34-1
Chemical Structure| 98600-34-1
Structure of 98600-34-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 98600-34-1 ]

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Product Details of [ 98600-34-1 ]

CAS No. :98600-34-1 MDL No. :MFCD05864695
Formula : C9H6BrNO Boiling Point : -
Linear Structure Formula :- InChI Key :IPAFHZDRYAWZOB-UHFFFAOYSA-N
M.W : 224.05 Pubchem ID :2763178
Synonyms :

Calculated chemistry of [ 98600-34-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.39
TPSA : 32.86 ?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) : -6.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.52
Log Po/w (XLOGP3) : 2.2
Log Po/w (WLOGP) : 2.74
Log Po/w (MLOGP) : 1.6
Log Po/w (SILICOS-IT) : 3.33
Consensus Log Po/w : 2.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.1
Solubility : 0.176 mg/ml ; 0.000787 mol/l
Class : Soluble
Log S (Ali) : -2.52
Solubility : 0.67 mg/ml ; 0.00299 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.09
Solubility : 0.0182 mg/ml ; 0.0000811 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.44

Safety of [ 98600-34-1 ]

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 [ 98600-34-1 ]

* 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 [ 98600-34-1 ]

[ 98600-34-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 98600-34-1 ]
  • [ 89245-35-2 ]
YieldReaction ConditionsOperation in experiment
49%
Stage #1: With sodium tetrahydroborate In methanol; formamide at 20℃; for 0.25 h;
Stage #2: at 55℃; for 16 h;
General procedure: To a flask containing a 3-formyl-indole derivative (1.0 equiv) and sodium borohydride (3.0 equiv), methanol (9mL for 1.0mmol of starting material) and formamide (9mL for 1.0mmol of starting material) were added and stirred at room temperature for 15min. The mixture was added to potassium cyanide (10.0 equiv) prepared in a separate flask and stirred at 55°C for 16h. The reaction was quenched by adding brine and a few drops of 5N NaOH, followed by extraction with dichloromethane thrice. The combined organic layer was washed with brine, dried over anhydrous sodium sulphate and concentrated in vacuo. Purification by flash silica gel column chromatography afforded the indole-3-acetonitrile derivative product.
Reference: [1] European Journal of Medicinal Chemistry, 2018, vol. 156, p. 344 - 367
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