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[ CAS No. 776-53-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 776-53-4
Chemical Structure| 776-53-4
Structure of 776-53-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 776-53-4 ]

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Product Details of [ 776-53-4 ]

CAS No. :776-53-4 MDL No. :MFCD00090781
Formula : C8H11N3O2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :QINRQIZOBCQKAZ-UHFFFAOYSA-N
M.W : 213.26 Pubchem ID :222666
Synonyms :

Calculated chemistry of [ 776-53-4 ]      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 : 54.24
TPSA : 103.4 ?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) : -6.56 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.96
Log Po/w (XLOGP3) : 1.47
Log Po/w (WLOGP) : 0.97
Log Po/w (MLOGP) : 0.33
Log Po/w (SILICOS-IT) : 0.9
Consensus Log Po/w : 1.12

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.14
Solubility : 1.54 mg/ml ; 0.00722 mol/l
Class : Soluble
Log S (Ali) : -3.25
Solubility : 0.12 mg/ml ; 0.000565 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.28
Solubility : 1.12 mg/ml ; 0.00525 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.0

Safety of [ 776-53-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280 UN#:
Hazard Statements:H317 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 776-53-4 ]

* 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 [ 776-53-4 ]

[ 776-53-4 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 4637-24-5 ]
  • [ 774-07-2 ]
  • [ 776-53-4 ]
  • 3
  • [ 774-07-2 ]
  • [ 74-88-4 ]
  • [ 776-53-4 ]
YieldReaction ConditionsOperation in experiment
97% In DMF (N,N-dimethyl-formamide); at 20 - 50℃; for 0.333333h; Iodomethane (2.6 g, 18 mmol) was added to the hot solution (50 C.) of ethyl 4-amino-2-mercaptopyrimidine-5-carboxylate (3.0 g, 15 mmol) in N,N-dimethylformamide (150 mL) and stirred at room temperature for 20 min. Solvent was removed in vacuo and the solid residue was washed by water. After dried in vacuo, desired product was obtained as a white solid (3.1 g, 97%). [0304] HPLC (4 minute gradient) tR=2.14 min; MS m/z 214.1 (M+H)+
45.2 g (86%) With potassium carbonate; In water; acetone; a) A mixture of 49 g (246 mmol) of 4-amino-5-carbethoxypyrimidine-2-thiol and 42 g (304 mmol) of potassium carbonate in 400 ml of acetone was treated with 50 g (352 mmol) of iodomethane. After stirring for 3 hours 500 ml of water were added. The phases were separated and the aqueous phase was extracted twice with 300 ml of dichloromethane each time. The combined organic phases were washed with 100 ml of brine, dried over magnesium sulfate, filtered and evaporated to give 45.2 g (86%) of ethyl 4-amino-2-methylthiopyrimidine-5-carboxylate as a pale yellow solid.
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