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[ CAS No. 2078-71-9 ] {[proInfo.proName]}

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Chemical Structure| 2078-71-9
Chemical Structure| 2078-71-9
Structure of 2078-71-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2078-71-9 ]

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Product Details of [ 2078-71-9 ]

CAS No. :2078-71-9 MDL No. :MFCD00059080
Formula : C3H8N2O2 Boiling Point : -
Linear Structure Formula :HOCH2CH2NHC(O)NH2 InChI Key :CLAHOZSYMRNIPY-UHFFFAOYSA-N
M.W : 104.11 Pubchem ID :73984
Synonyms :

Calculated chemistry of [ 2078-71-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.67
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 3.0
Molar Refractivity : 23.79
TPSA : 75.35 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -8.16 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.38
Log Po/w (XLOGP3) : -1.72
Log Po/w (WLOGP) : -1.35
Log Po/w (MLOGP) : -1.29
Log Po/w (SILICOS-IT) : -1.45
Consensus Log Po/w : -1.09

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.8
Solubility : 651.0 mg/ml ; 6.25 mol/l
Class : Highly soluble
Log S (Ali) : 0.65
Solubility : 466.0 mg/ml ; 4.48 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : 0.32
Solubility : 216.0 mg/ml ; 2.07 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.02

Safety of [ 2078-71-9 ]

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 [ 2078-71-9 ]

* 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 [ 2078-71-9 ]

[ 2078-71-9 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 75-21-8 ]
  • [ 57-13-6 ]
  • [ 497-25-6 ]
  • [ 2078-71-9 ]
  • [ 142-27-8 ]
  • 2
  • [ 75-21-8 ]
  • [ 57-13-6 ]
  • [ 2078-71-9 ]
  • [ 142-27-8 ]
  • 3
  • [ 2078-71-9 ]
  • [ 42466-67-1 ]
  • 6-amino-1-(2-hydroxy-ethyl)-2-oxo-1,2-dihydro-pyrimidine-5-carboxylic acid ethyl ester [ No CAS ]
  • 4
  • [ 2078-71-9 ]
  • [ 40380-05-0 ]
  • 5
  • [ 2078-71-9 ]
  • [ 122-04-3 ]
  • 4-nitro-benzoic acid-(2-ureido-ethyl ester) [ No CAS ]
  • 6
  • [ 2078-71-9 ]
  • [ 122-51-0 ]
  • [ 109-77-3 ]
  • <i>N</i>-(2,2-dicyano-vinyl)-<i>N</i>'-(2-hydroxy-ethyl)-urea [ No CAS ]
  • 7
  • [ 2078-71-9 ]
  • [ 122-51-0 ]
  • [ 105-34-0 ]
  • [ 116865-90-8 ]
  • 8
  • [ 2078-71-9 ]
  • [ 105-56-6 ]
  • [ 56075-69-5 ]
YieldReaction ConditionsOperation in experiment
59.4% With sodium; In ethanol;Cooling with ice; Reflux; Synthesis of 1-hydroxy-ethyl-6-aminouracil (compound 1) Metal sodium (2.8 g, 120 mmol) was added carefully in 90 mL of ethanol anhydride in a 200 mL mad apple-type flask with a stirrer coated with fluoropolymer in ice bath with constant stirring and was completely dissolved. Then, 6.3 g (60 mmol) of hydroxyethylurea and 6.4 mL (60 mmol) of ethylcyanoacetate were added and refluxed for seven hr. The obtained solution was filtrated, washed with ethanol, solubilized in water, neutralized with 1.0 M diluted hydrochloric acid, filtrated and provided white pellets, which were recrystallized in water and gave compound 1 as a white crystal (6.1 g, 35.6 mmol, yield: 59.4percent); 1H NMR (DMSO-d6, 400 MHz): delta 3.54 (t, 2H, NCH2CH2, 9.6 Hz), 3.83 (t, 2H, CH2OH, 9.6 Hz), 4.57 (br, 1H, CHCNH2), 5.09 (br, 1H, OH), 6.61 (br, 2H, NH2), 10.32 (br, 1H, NH); 13C NMR (DMSO-d6, 100 MHz): delta 44.13 (NaC2CH2), 59.28 (CH2OH), 76.52 (CHCNH2), 151.87, 157.04, 162.89.
  • 9
  • [ 2078-71-9 ]
  • [ 102-92-1 ]
  • <i>N</i>-(2-<i>trans</i>-cinnamoyloxy-ethyl)-<i>N</i>'-<i>trans</i>-cinnamoyl-urea [ No CAS ]
  • 10
  • [ 2078-71-9 ]
  • [ 119-67-5 ]
  • [ 100061-11-8 ]
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