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[ CAS No. 364-30-7 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 364-30-7
Chemical Structure| 364-30-7
Chemical Structure| 364-30-7
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Product Details of [ 364-30-7 ]

CAS No. :364-30-7 MDL No. :MFCD00034058
Formula : C6H4F2N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :WPEUQAOOZXFRKZ-UHFFFAOYSA-N
M.W : 174.11 Pubchem ID :9697
Synonyms :

Calculated chemistry of [ 364-30-7 ]

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 39.58
TPSA : 71.84 Ų

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) : -6.07 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.15
Log Po/w (XLOGP3) : 1.82
Log Po/w (WLOGP) : 2.3
Log Po/w (MLOGP) : 1.15
Log Po/w (SILICOS-IT) : -0.14
Consensus Log Po/w : 1.26

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.37
Solubility : 0.743 mg/ml ; 0.00427 mol/l
Class : Soluble
Log S (Ali) : -2.95
Solubility : 0.196 mg/ml ; 0.00113 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.97
Solubility : 1.85 mg/ml ; 0.0106 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.99

Safety of [ 364-30-7 ]

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 [ 364-30-7 ]

* 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.

  • Upstream synthesis route of [ 364-30-7 ]
  • Downstream synthetic route of [ 364-30-7 ]

[ 364-30-7 ] Synthesis Path-Upstream   1~9

  • 1
  • [ 364-30-7 ]
  • [ 2106-40-3 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
[3] Journal of the American Chemical Society, 1951, vol. 73, p. 153[4] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 2
  • [ 364-30-7 ]
  • [ 315-14-0 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
[3] Journal of the American Chemical Society, 1951, vol. 73, p. 153[4] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 3
  • [ 364-30-7 ]
  • [ 1435-43-4 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 4
  • [ 364-30-7 ]
  • [ 363-69-9 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
[3] Journal of the American Chemical Society, 1951, vol. 73, p. 153[4] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 5
  • [ 441-30-5 ]
  • [ 364-30-7 ]
Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 9, p. 1375 - 1384
[2] European Journal of Medicinal Chemistry, 2009, vol. 44, # 7, p. 2930 - 2935
[3] Journal of Heterocyclic Chemistry, 2009, vol. 46, # 5, p. 980 - 987
  • 6
  • [ 399-36-0 ]
  • [ 364-30-7 ]
Reference: [1] Journal of Fluorine Chemistry, 2003, vol. 121, # 2, p. 171 - 175
[2] Journal of the American Chemical Society, 1951, vol. 73, p. 153[3] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 7
  • [ 367-25-9 ]
  • [ 364-30-7 ]
Reference: [1] Journal of Fluorine Chemistry, 2003, vol. 121, # 2, p. 171 - 175
  • 8
  • [ 364-30-7 ]
  • [ 372-39-4 ]
Reference: [1] Journal of the American Chemical Society, 1951, vol. 73, p. 153[2] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
  • 9
  • [ 364-30-7 ]
  • [ 2369-29-1 ]
YieldReaction ConditionsOperation in experiment
46% for 1.5 h; Reflux Concentrated hydrochloric acid (10 mL) was slowly added dropwise to a mixture of difluoronitroaniline 7 (1.6 g, 9 mmol) and tin (22.5mmol). The reaction mixture was heated at reflux for 1.5 h, cooled tor.t., and neutralized with 50percent NaOH solution to pH 9–10. The precipitate was filtered, dried, and extracted with hot EtOAc (80 mL). Afterevaporation of the filtrate, diamine 9 was obtained.Yield: 0.60 g (46percent); brown crystals; mp 55–57 °C; Rf 0.86.
Reference: [1] Tetrahedron Letters, 2006, vol. 47, # 27, p. 4591 - 4595
[2] European Journal of Medicinal Chemistry, 2009, vol. 44, # 7, p. 2930 - 2935
[3] Synthesis (Germany), 2016, vol. 48, # 3, p. 394 - 406
[4] Journal of the American Chemical Society, 1951, vol. 73, p. 153[5] Journal of the American Chemical Society, 1959, vol. 81, p. 94,98
[6] Journal of Medicinal Chemistry, 1995, vol. 38, # 25, p. 4906 - 4916
[7] Patent: US2002/132842, 2002, A1,
[8] Patent: US2012/122837, 2012, A1, . Location in patent: Page/Page column 75
[9] Journal of Medicinal Chemistry, 2015, vol. 58, # 1, p. 362 - 375
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