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[ CAS No. 53554-29-3 ] {[proInfo.proName]}

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Chemical Structure| 53554-29-3
Chemical Structure| 53554-29-3
Structure of 53554-29-3 * Storage: {[proInfo.prStorage]}

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Product Details of [ 53554-29-3 ]

CAS No. :53554-29-3 MDL No. :MFCD00023234
Formula : C8H10N2O3S Boiling Point : No data available
Linear Structure Formula :- InChI Key :HDIWKNXVBQPJCO-UHFFFAOYSA-N
M.W : 214.24 Pubchem ID :239049
Synonyms :

Calculated chemistry of [ 53554-29-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.38
Num. rotatable bonds : 4
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 52.67
TPSA : 97.35 ?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) : -7.15 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.6
Log Po/w (XLOGP3) : 0.65
Log Po/w (WLOGP) : 0.67
Log Po/w (MLOGP) : 0.38
Log Po/w (SILICOS-IT) : 1.77
Consensus Log Po/w : 1.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.63
Solubility : 5.01 mg/ml ; 0.0234 mol/l
Class : Very soluble
Log S (Ali) : -2.27
Solubility : 1.15 mg/ml ; 0.00537 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.55
Solubility : 0.609 mg/ml ; 0.00284 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.01

Safety of [ 53554-29-3 ]

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

Application In Synthesis of [ 53554-29-3 ]

* 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 [ 53554-29-3 ]

[ 53554-29-3 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 124-40-3 ]
  • [ 53554-29-3 ]
  • [ 54127-88-7 ]
  • 2
  • [ 74-89-5 ]
  • [ 53554-29-3 ]
  • [ 84331-97-5 ]
  • 4
  • [ 2986-19-8 ]
  • [ 87-13-8 ]
  • [ 53554-29-3 ]
YieldReaction ConditionsOperation in experiment
99.7% S1, methylthiourea sulfate(75.2g, 0.4mol)Add to a mass fraction of 16% NaOH (250 mL, 1.18 mol) and stir for 30 min.Then diethyl ethoxymethylenemalonate (103.4 g, 0.48 mol)Soluble in 160mL of ethanol and slowly drip into the reaction solution,After the completion of the dropwise addition, the reaction was carried out at room temperature for 10 hours, when a large amount of white solid precipitated,Pumping,Washed,Drying in vacuo gave a white solid (84.7 g, 99.7%);
87.6% With sodium ethanolate; In ethanol; at 20℃; for 3h; To a solution of 2-ethoxymethylenemalonic acid diethyl ester (59.0 g, 273 mmol) in EtOH (300 mL) was added 2-methyl-isothiourea (41.5 g, 150 mmol) in an ice-H2O bath. An EtOHic solution of EtONa (2M, 300 mL) was added dropwise maintaining the reaction temperature under 5 C. The mixture was warmed to RT and stirred for 3h. After standing overnight, the solvent was removed under reduced pressure and the residue was dissolved in H2O (800 mL) at 0 C. The solution was acidified to pH 3 with cone. HCl and the precipitate collected by filtration and air-dried to yield 4-hydroxy-2- methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester as a white solid (50.8 g, 87.6% yield).
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