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[ CAS No. 77770-09-3 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 77770-09-3
Chemical Structure| 77770-09-3
Chemical Structure| 77770-09-3
Structure of 77770-09-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 77770-09-3 ]

CAS No. :77770-09-3 MDL No. :MFCD03095407
Formula : C7H8INO Boiling Point : -
Linear Structure Formula :- InChI Key :KCAGMESWEMVFON-UHFFFAOYSA-N
M.W : 249.05 Pubchem ID :12905382
Synonyms :

Calculated chemistry of [ 77770-09-3 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.06
TPSA : 35.25 Ų

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) : -6.38 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.92
Log Po/w (XLOGP3) : 2.03
Log Po/w (WLOGP) : 1.89
Log Po/w (MLOGP) : 2.06
Log Po/w (SILICOS-IT) : 2.07
Consensus Log Po/w : 2.0

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.04
Solubility : 0.227 mg/ml ; 0.00091 mol/l
Class : Soluble
Log S (Ali) : -2.4
Solubility : 0.996 mg/ml ; 0.004 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.12
Solubility : 0.188 mg/ml ; 0.000757 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.03

Safety of [ 77770-09-3 ]

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 [ 77770-09-3 ]

* 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 [ 77770-09-3 ]
  • Downstream synthetic route of [ 77770-09-3 ]

[ 77770-09-3 ] Synthesis Path-Upstream   1~4

  • 1
  • [ 77770-09-3 ]
  • [ 5399-03-1 ]
Reference: [1] Journal of the Chemical Society, 1916, vol. 109, p. 1087
  • 2
  • [ 52692-09-8 ]
  • [ 77770-09-3 ]
YieldReaction ConditionsOperation in experiment
66% With tin(II) chloride dihdyrate In ethanol; ethyl acetate at 70℃; for 0.5 h; Inert atmosphere A dry nitrogen-flushed round bottom flask, equipped with a magnetic stirrer was charged with amixture of 3-nitro-4-methoxyphenyl iodide (16.2 g, 58 mmol) and SnCl2·2H2O (65.5 g, 290 mmol) in75 ml of EtOH and 30 ml of EtOAc. The reaction was heated at 70 °C for 30 min. Half of the solvents was evaporated and 100 ml of Et2O was added. The mixture was left in the fridge over the night. The obtained precipitate was filtered and washed with Et2O. The solid was dissolved in 150 mlof 15percent NaOH cooled in an ice bath. The mixture was extracted with CH2Cl2, the organic layers were washed with brine, dried over Na2SO4 and concentrated to 3-amino-4-methoxyphenyl iodide (9.5 g,38 mmol, 66percent) as a white solid.
Reference: [1] Synlett, 2012, vol. 23, # 8, p. 1205 - 1208
[2] Synlett, 2013, vol. 24, # 14, p. 1772 - 1776
[3] Russian Chemical Bulletin, 2013, vol. 62, # 4, p. 1103 - 1110[4] Izv. Akad. Nauk, Ser. Khim., 2013, # 4, p. 1102 - 1110,9
[5] Journal of the Chemical Society, 1916, vol. 109, p. 1087
  • 3
  • [ 696-62-8 ]
  • [ 77770-09-3 ]
Reference: [1] Journal of the American Chemical Society, 2013, vol. 135, # 13, p. 5000 - 5003
  • 4
  • [ 91-23-6 ]
  • [ 77770-09-3 ]
Reference: [1] Journal of the Chemical Society, 1916, vol. 109, p. 1087
[2] Synlett, 2012, vol. 23, # 8, p. 1205 - 1208
[3] Synlett, 2013, vol. 24, # 14, p. 1772 - 1776
[4] Russian Chemical Bulletin, 2013, vol. 62, # 4, p. 1103 - 1110[5] Izv. Akad. Nauk, Ser. Khim., 2013, # 4, p. 1102 - 1110,9
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