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[ CAS No. 591-54-8 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 591-54-8
Chemical Structure| 591-54-8
Structure of 591-54-8 * Storage: {[proInfo.prStorage]}
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Product Details of [ 591-54-8 ]

CAS No. :591-54-8 MDL No. :MFCD00006112
Formula : C4H5N3 Boiling Point : -
Linear Structure Formula :- InChI Key :OYRRZWATULMEPF-UHFFFAOYSA-N
M.W : 95.10 Pubchem ID :68958
Synonyms :

Calculated chemistry of [ 591-54-8 ]

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 26.44
TPSA : 51.8 Ų

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) : -7.06 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.8
Log Po/w (XLOGP3) : -0.25
Log Po/w (WLOGP) : 0.07
Log Po/w (MLOGP) : -0.72
Log Po/w (SILICOS-IT) : 0.38
Consensus Log Po/w : 0.05

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.91
Solubility : 11.8 mg/ml ; 0.124 mol/l
Class : Very soluble
Log S (Ali) : -0.38
Solubility : 39.7 mg/ml ; 0.417 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.21
Solubility : 5.93 mg/ml ; 0.0624 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.22

Safety of [ 591-54-8 ]

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 [ 591-54-8 ]

* 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 [ 591-54-8 ]

[ 591-54-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 591-54-8 ]
  • [ 759-02-4 ]
  • [ 100-52-7 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
With zinc(II) nitrate In acetonitrile at 120℃; for 0.5h; Microwave irradiation; General procedure for one-pot and two-step α-fluorinated carbonyl compounds followed by the Mannich reaction General procedure: The ethyl 3-oxo-3-phenylpropanoate (96 mg, 0.5 mmol) was added to a solution of SelectfluorTM, (Sigma, 177 mg, 0.5 mmol) in CH3CN (1.0 mL). After heating in a Biotage Initiator microwave reactor at 90 °C for 30 min. The benzaldehyde (53 mg, 0.5 mmol), aniline (46 mg, 0.5 mmol) and Zn(NO3)2 (19 mg, 20 mol%) were carefully added to the fluorinated solution and placed in microwave reactor at 120 °C for another 30 min. The reaction mixture was purified by flash column chromatography on silica gel giving the fluorinated product 3ac
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