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[ CAS No. 321-28-8 ] {[proInfo.proName]}

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Chemical Structure| 321-28-8
Chemical Structure| 321-28-8
Structure of 321-28-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 321-28-8 ]

CAS No. :321-28-8 MDL No. :MFCD00000316
Formula : C7H7FO Boiling Point : -
Linear Structure Formula :- InChI Key :JIXDOBAQOWOUPA-UHFFFAOYSA-N
M.W : 126.13 Pubchem ID :67576
Synonyms :

Calculated chemistry of [ 321-28-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 32.89
TPSA : 9.23 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.55 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.93
Log Po/w (XLOGP3) : 2.14
Log Po/w (WLOGP) : 2.25
Log Po/w (MLOGP) : 2.24
Log Po/w (SILICOS-IT) : 2.26
Consensus Log Po/w : 2.17

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.4
Solubility : 0.505 mg/ml ; 0.004 mol/l
Class : Soluble
Log S (Ali) : -1.97
Solubility : 1.36 mg/ml ; 0.0108 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.76
Solubility : 0.218 mg/ml ; 0.00173 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 321-28-8 ]

Signal Word:Danger Class:3
Precautionary Statements:P210-P403+P235 UN#:1993
Hazard Statements:H225 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 321-28-8 ]

* 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 [ 321-28-8 ]

[ 321-28-8 ] Synthesis Path-Downstream   1~10

  • 1
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  • [ 344-78-5 ]
  • [ 455-93-6 ]
  • 2
  • [ 321-28-8 ]
  • [ 455-93-6 ]
YieldReaction ConditionsOperation in experiment
In ethanol; water; acetic anhydride; 2-Fluoro-4-nitroanisole (IX) To a cold (-2), stirred solution of 285 g. (2.26 mol) of 2-fluoroanisole in 1.1 L of acetic anhydride was added, dropwise, 114 mL of fuming nitric acid (sp. gr. 1.59) at such a rate that the reaction temperature remained between -2 and 0. The reaction mixture was stirred for 5 hours at this temperature then poured into 4.0 L of water. The suspension was stirred for 1.5 hours, stored for 15 hours, then extracted with methylene chloride (2*1.0 L). The combined extracts were washed with water (2*500 mL), dried over anhydrous magnesium sulfate, then concentrated in vacuo (475 g.). Crystallization from ethanol gave 147.4 g. (38%) of material suitable for further transformation. Additional material (34.5 g.) was obtained from three scouting runs. Analytically pure product (5.2 g.; 63.4% recovery) was obtained by recrystallizing 8.2 g of the material from 200 mL of ethanol; mp, 105-106 (Literature, R. C. Elderfield et al., J. Am. Chem. Soc., 68, 1584 (1946)). Anal. Calcd for C7 H6 FNO3 (percent): C, 49.13; H, 3.53; F, 11.10; N, 8.19. Found: C, 49.07; H, 3.52; F, 11.02; N, 8.19.
  • 3
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  • [ 151-50-8 ]
  • [ 331-62-4 ]
  • 5
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  • [ 455-93-6 ]
  • [ 484-94-6 ]
  • 6
  • [ 321-28-8 ]
  • [ 7697-37-2 ]
  • [ 108-24-7 ]
  • [ 455-93-6 ]
  • 7
  • [ 321-28-8 ]
  • [ 7697-37-2 ]
  • [ 344-78-5 ]
  • [ 455-93-6 ]
  • 8
  • [ 4224-62-8 ]
  • [ 321-28-8 ]
  • 6-chloro-1-(3-fluoro-4-methoxyphenyl)-hexan-1-one [ No CAS ]
  • 9
  • 4-methoxy-2-methylphenyl(2-methoxyphenyl)iodonium trifluoroacetate [ No CAS ]
  • [ 321-28-8 ]
  • [ 2338-54-7 ]
  • 10
  • [ 321-28-8 ]
  • [ 331-62-4 ]
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