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[ CAS No. 771-51-7 ] {[proInfo.proName]}

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Chemical Structure| 771-51-7
Chemical Structure| 771-51-7
Structure of 771-51-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 771-51-7 ]

CAS No. :771-51-7 MDL No. :MFCD00005628
Formula : C10H8N2 Boiling Point : -
Linear Structure Formula :- InChI Key :DMCPFOBLJMLSNX-UHFFFAOYSA-N
M.W : 156.18 Pubchem ID :351795
Synonyms :
Chemical Name :2-(1H-Indol-3-yl)acetonitrile

Calculated chemistry of [ 771-51-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.1
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.82
TPSA : 39.58 ?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) : -6.12 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.33
Log Po/w (XLOGP3) : 1.6
Log Po/w (WLOGP) : 2.23
Log Po/w (MLOGP) : 1.18
Log Po/w (SILICOS-IT) : 2.82
Consensus Log Po/w : 1.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.31
Solubility : 0.773 mg/ml ; 0.00495 mol/l
Class : Soluble
Log S (Ali) : -2.04
Solubility : 1.42 mg/ml ; 0.00906 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.76
Solubility : 0.0271 mg/ml ; 0.000174 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.36

Safety of [ 771-51-7 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P501-P261-P270-P271-P264-P280-P361+P364-P301+P310+P330-P302+P352+P312-P304+P340+P311-P403+P233-P405 UN#:3439
Hazard Statements:H301-H311-H331 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 771-51-7 ]

* 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.

  • Downstream synthetic route of [ 771-51-7 ]

[ 771-51-7 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 700-06-1 ]
  • [ 143-33-9 ]
  • [ 771-51-7 ]
  • 2
  • [ 700-06-1 ]
  • [ 151-50-8 ]
  • [ 771-51-7 ]
  • 3
  • glucobrassicin [ No CAS ]
  • [ 700-06-1 ]
  • [ 771-51-7 ]
  • [ 1968-05-4 ]
  • 4
  • [ 771-51-7 ]
  • [ 10273-40-2 ]
  • (Z)-2-(1H-indol-3-yl)-3-(2,7-naphthyridine-4-yl)acrylonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
24% General procedure: To an indole-3-acetonitrile derivative (1.0 equiv) dissolved in anhydrous methanol (4mL for 2.31mmol of starting material) in a dried microwave vial, sodium methoxide (1.7 equiv) was added and stirred at room temperature for 15min protected from light. Quinoline/isoquinoline-carboxaldehyde derivative (1.2 equiv) was added and the mixture was subjected to microwave irradiation at 95C for 8.5min. The reaction was cooled to room temperature and then chilled in an ice/salt bath. The resulting precipitate was filtered, washed with methanol, and dried under vacuum to afford a solid as the product.
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