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[ CAS No. 1072-83-9 ] {[proInfo.proName]}

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Chemical Structure| 1072-83-9
Chemical Structure| 1072-83-9
Structure of 1072-83-9 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1072-83-9 ]

CAS No. :1072-83-9 MDL No. :MFCD00005220
Formula : C6H7NO Boiling Point : No data available
Linear Structure Formula :HNC4H3C(O)CH3 InChI Key :IGJQUJNPMOYEJY-UHFFFAOYSA-N
M.W : 109.13 Pubchem ID :14079
Synonyms :
Chemical Name :1-(1H-Pyrrol-2-yl)ethanone

Calculated chemistry of [ 1072-83-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 30.99
TPSA : 32.86 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.45 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.06
Log Po/w (XLOGP3) : 0.73
Log Po/w (WLOGP) : 1.22
Log Po/w (MLOGP) : -0.18
Log Po/w (SILICOS-IT) : 1.71
Consensus Log Po/w : 0.91

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.37
Solubility : 4.62 mg/ml ; 0.0424 mol/l
Class : Very soluble
Log S (Ali) : -1.0
Solubility : 10.9 mg/ml ; 0.1 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.88
Solubility : 1.44 mg/ml ; 0.0132 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.06

Safety of [ 1072-83-9 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1072-83-9 ]

* 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 [ 1072-83-9 ]

[ 1072-83-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1072-83-9 ]
  • [ 14150-94-8 ]
  • [ 1203570-45-9 ]
  • 2
  • chitosan, Mw = 760000, degree of deacetylation DD = 85.5%, [ No CAS ]
  • [ 109-08-0 ]
  • [ 1122-62-9 ]
  • [ 1192-62-7 ]
  • [ 2214-53-1 ]
  • [ 85279-30-7 ]
  • [ 1072-83-9 ]
  • [ 1262900-24-2 ]
  • [ 99969-04-7 ]
  • [ 32736-95-1 ]
  • [ 74376-36-6 ]
  • 3
  • [ 1072-83-9 ]
  • [ 133730-34-4 ]
  • C14H15NO3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With nickel(II) oxide; potassium carbonate; In ethanol; water; at 50℃; for 24h; General procedure: The general procedure for C-N coupling involves stirringthe mixture of phenyl boronic acid (1mmol), nucleophileslike pyrrole or indole (1.5mmol) and NiO catalyst (7mg)in 5ml of solvent at 50C. The progress of the reactionwas monitored by thin layer chromatography (TLC) using petroleum ether and ethyl acetate as eluting solvents. Afterthe completion of reaction, the reaction mixture was mixedwith 15ml distilled water and 15ml ethyl acetate to separatethe aqueous and organic layers. The resulting organic layerswere collected together, washed and dried. The raw productwas separated by preparative thin layer chromatographyusing the same eluents petroleum ether and ethyl acetate.The formation of N-arylated products were confirmed byNMR and GC-MS analysis.
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