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[ CAS No. 1480-96-2 ] {[proInfo.proName]}

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Chemical Structure| 1480-96-2
Chemical Structure| 1480-96-2
Structure of 1480-96-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1480-96-2 ]

CAS No. :1480-96-2 MDL No. :MFCD03265437
Formula : C5H5FN2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :VMIFBCPINLZNNI-UHFFFAOYSA-N
M.W : 144.10 Pubchem ID :352550
Synonyms :

Calculated chemistry of [ 1480-96-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.2
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 31.31
TPSA : 54.98 ?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) : -7.19 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.3
Log Po/w (XLOGP3) : -0.01
Log Po/w (WLOGP) : 0.34
Log Po/w (MLOGP) : 0.02
Log Po/w (SILICOS-IT) : 1.5
Consensus Log Po/w : 0.63

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.11
Solubility : 11.3 mg/ml ; 0.0785 mol/l
Class : Very soluble
Log S (Ali) : -0.7
Solubility : 29.1 mg/ml ; 0.202 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.94
Solubility : 1.64 mg/ml ; 0.0114 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.93

Safety of [ 1480-96-2 ]

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 [ 1480-96-2 ]

* 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 [ 1480-96-2 ]

[ 1480-96-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1480-96-2 ]
  • [ 1801-06-5 ]
YieldReaction ConditionsOperation in experiment
95% With triethylamine; trichlorophosphate; In toluene; at 50 - 80℃; The 14.4g type IV compounds add 29 ml of toluene and 15.2g in triethylamine, heating to 50-80°C, dropwise 18.4g phosphorus oxychloride, the drop finishes, preserving heat and stirring reaction 5-7 hours, cooling to room temperature, adding water, separating, collecting the organic phase, organic phase is concentrated under reduced pressure, compound III namely type (strawcoloured liquid) 15.4g, molar yield is 95.0percent, HPLC purity of 95.8percent.
34% With N,N-dimethyl-aniline; trichlorophosphate; at 110℃; for 1.5h; 43b2-Methoxy-5-fluorouracil (43a, 1.04g, 7.21 mmol) and N,N-dimethylaniline (1.80 mL) were heated in POCI3 at 11O0C for 90 minutes. After cooling, the reaction was added carefully to ice. The product was extracted with diethylether. The ether layer was washed with sequentially with 2N HCI, water, and brine followed by drying (MgSO4). The ether was carefully removed under reduced pressure to give 43b as a volatile liquid (0.39g, 34percent) which was used without further purification. Rf = 0.26 (10percent EtOAc/hexane). 1H NMR (400MHz, DMSO-d6): delta 3.91 (s, 3H), 8.79 (s, 1 H)
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