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[ CAS No. 13304-62-6 ] {[proInfo.proName]}

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Chemical Structure| 13304-62-6
Chemical Structure| 13304-62-6
Structure of 13304-62-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 13304-62-6 ]

CAS No. :13304-62-6 MDL No. :MFCD00015333
Formula : C10H11NO Boiling Point : No data available
Linear Structure Formula :- InChI Key :OHLHOLGYGRKZMU-UHFFFAOYSA-N
M.W : 161.20 Pubchem ID :139428
Synonyms :

Calculated chemistry of [ 13304-62-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.1
Num. rotatable bonds : 4
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.36
TPSA : 29.1 ?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) : -6.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.98
Log Po/w (XLOGP3) : 1.54
Log Po/w (WLOGP) : 1.34
Log Po/w (MLOGP) : 1.79
Log Po/w (SILICOS-IT) : 2.05
Consensus Log Po/w : 1.74

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.92
Solubility : 1.96 mg/ml ; 0.0121 mol/l
Class : Very soluble
Log S (Ali) : -1.76
Solubility : 2.8 mg/ml ; 0.0174 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.24
Solubility : 0.0934 mg/ml ; 0.000579 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.03

Safety of [ 13304-62-6 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P301+P310-P305+P351+P338-P405-P501 UN#:2811
Hazard Statements:H301-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 13304-62-6 ]

* 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 [ 13304-62-6 ]

[ 13304-62-6 ] Synthesis Path-Downstream   1~12

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YieldReaction ConditionsOperation in experiment
86.8% With sulfuric acid; at 10 - 60℃; EXAMPLE 1 Step 1 N-Benzyl acrylamideTo acrylonitrile, 318.8g (6 mol) is added sulfuric acid, 235g (2.4 mol) keeping the temperature below 10C. Benzyl alcohol, 216.3g (2 mol) is slowly added below 10C. The mixture is heated to 60C and stirred until the benzyl alcohol is consumed. The mixture is cooled to ca 25C and toluene, 173g, is added. The product solution is washed with 300g of water followed by 2 x 100g of 10 % sodium carbonate. The toluene is stripped at reduced pressure and the product 280g, 86.8 % yield, is isolated as an oil that solidifies upon standing.
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  • [ 96130-96-0 ]
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  • [ 101502-01-6 ]
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YieldReaction ConditionsOperation in experiment
70% A solution of acrylic acid (2, 0.95 mL, 13.8 mmol), HOBt (2.06 g,15.2 mmol), and EDCI (2.92 g, 15.2 mmol) in anhyd CH2Cl2 (20 mL) was stirred at 0 C under a N2 atmosphere for 15 min. This mixture was treated with benzylamine (3, 1.73 mL, 16.6 mmol) and Et3N (3.8 mL, 27.7 mmol) and stirred for an additional 8 h. The mixture was quenched with sat. NH4Cl soln (20 mL) and after 10 min, extracted with CH2Cl2 (2 × 25 mL). The combined organic layers were washed with H2O (20 mL), NaHCO3 soln (20 mL), and brine (25 mL), dried (Na2SO4), and evaporated under reduced pressure. The obtained residue was purified by column chromatography (60-120 mesh silica gel, EtOAc-hexane, 2:8) to afford pure 4 (1.56 g, 70%) as a solid; mp 58-59 C.
  • 7
  • [ 814-68-6 ]
  • [ 100-46-9 ]
  • [ 13304-62-6 ]
Reference: [1]Angewandte Chemie - International Edition,2013,vol. 52,p. 5818 - 5821
    Angew. Chem.,2013,vol. 125,p. 5930 - 5933,4
[2]Journal of Medicinal Chemistry,2014,vol. 57,p. 7590 - 7599
[3]MedChemComm,2019,vol. 10,p. 1109 - 1115
[4]ChemSusChem,2013,vol. 6,p. 905 - 910
[5]Angewandte Chemie - International Edition,2018,vol. 57,p. 8854 - 8858
    Angew. Chem.,2018,vol. 130,p. 8992 - 8996,5
[6]Chemical Communications,2012,vol. 48,p. 11232 - 11234
[7]European Journal of Organic Chemistry,2007,p. 455 - 461
[8]Beilstein Journal of Organic Chemistry,2010,vol. 6
[9]Organic and Biomolecular Chemistry,2005,vol. 3,p. 2175 - 2182
[10]Chemical Communications,2017,vol. 53,p. 7234 - 7237
[11]Angewandte Chemie - International Edition,2019,vol. 58,p. 10747 - 10751
    Angew. Chem.,2019,vol. 131,p. 10858 - 10863,6
[12]Angewandte Chemie - International Edition,2020,vol. 59,p. 5193 - 5201
    Angew. Chem.,2020,vol. 132,p. 5231 - 5239,9
[13]Journal of medicinal and pharmaceutical chemistry,1961,vol. 4,p. 259 - 296
[14]Organic Letters,2003,vol. 5,p. 4029 - 4031
[15]Journal of Organic Chemistry,2003,vol. 68,p. 6360 - 6368
[16]Journal of Organic Chemistry,2005,vol. 70,p. 7810 - 7815
[17]Journal of Organic Chemistry,2010,vol. 75,p. 3047 - 3052
[18]Helvetica Chimica Acta,2013,vol. 96,p. 1355 - 1365
[19]Russian Journal of Organic Chemistry,2013,vol. 49,p. 1690 - 1702
    Zh. Org. Khim.,2013,vol. 49,p. 1707 - 1718,12
[20]Angewandte Chemie - International Edition,2015,vol. 54,p. 4246 - 4249
    Angew. Chem.,2015,vol. 127,p. 4320 - 4323
[21]Chemistry - A European Journal,2015,vol. 21,p. 18961 - 18965
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