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[ CAS No. 5438-70-0 ] {[proInfo.proName]}

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Chemical Structure| 5438-70-0
Chemical Structure| 5438-70-0
Structure of 5438-70-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 5438-70-0 ]

CAS No. :5438-70-0 MDL No. :MFCD00017569
Formula : C10H13NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :CFNDVXUTYPXOPG-UHFFFAOYSA-N
M.W : 179.22 Pubchem ID :225219
Synonyms :

Calculated chemistry of [ 5438-70-0 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.3
Num. rotatable bonds : 4
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.52
TPSA : 52.32 ?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) : -6.26 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.67
Log Po/w (XLOGP3) : 1.6
Log Po/w (WLOGP) : 1.38
Log Po/w (MLOGP) : 1.67
Log Po/w (SILICOS-IT) : 1.67
Consensus Log Po/w : 1.6

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.04
Solubility : 1.65 mg/ml ; 0.00919 mol/l
Class : Soluble
Log S (Ali) : -2.31
Solubility : 0.877 mg/ml ; 0.0049 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.92
Solubility : 0.214 mg/ml ; 0.00119 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 1.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.46

Safety of [ 5438-70-0 ]

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

Application In Synthesis of [ 5438-70-0 ]

* 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 [ 5438-70-0 ]

[ 5438-70-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 18740-39-1 ]
  • [ 5438-70-0 ]
  • [ 1436866-42-0 ]
YieldReaction ConditionsOperation in experiment
45% In N,N-dimethyl-formamide; at 65℃; for 2.5h; To a solution of 1H-thieno[2,3-d]pyrimidine-2,4-dione (62) (92.8 mg, 0.552 mmol) in toluene (1 mL) were added N,N-dimethylaniline (0.140 mL, 1.10 mmol) and phosphoryl chloride (0.280 mL, 3.00 mmol). The reaction mixture was warmed to 100 °C and stirred for 3 h. After cooling to room temperature, H2O was added to the reaction mixture and the mixture was extracted with CHCl3. The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo to give <strong>[18740-39-1]2,4-dichlorothieno[2,3-d]pyrimidine</strong> (63). This compound was used for the next reaction without further purification.To a solution of 63 in DMF (4 mL) was added ethyl 2-(4-aminophenyl)acetate (95.2 mg, 0.531 mmol) and the reaction mixture was stirred at 65 °C for 2.5 h. After cooling, H2O was added to the reaction mixture and the mixture was extracted with EtOAc. The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was chromatographed (EtOAc/hexane = 0percent to 100percent) to give the title compound (85.9 mg, 0.247 mmol, 45percent) as a colorless solid. 1H NMR (CDCl 3) delta: 1.28 (3H, t, J = 7.4 Hz), 3.64 (2H, s), 4.18 (2H, q, J = 7.4 Hz), 7.03 (1H, d, J = 5.7 Hz), 7.21 (1H, s), 7.29 (1H, d, J = 5.7 Hz), 7.32 (2H, d, J = 8.6 Hz), 7.56 (2H, d, J = 8.6 Hz).
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