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[ CAS No. 773869-57-1 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 773869-57-1
Chemical Structure| 773869-57-1
Chemical Structure| 773869-57-1
Structure of 773869-57-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 773869-57-1 ]

CAS No. :773869-57-1 MDL No. :MFCD06202863
Formula : C7H7IO2 Boiling Point : -
Linear Structure Formula :- InChI Key :VIWWSAGABDIIFF-UHFFFAOYSA-N
M.W : 250.03 Pubchem ID :18525941
Synonyms :

Calculated chemistry of [ 773869-57-1 ]

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 47.31
TPSA : 40.46 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 : Yes
Log Kp (skin permeation) : -6.88 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.81
Log Po/w (XLOGP3) : 1.33
Log Po/w (WLOGP) : 1.34
Log Po/w (MLOGP) : 1.8
Log Po/w (SILICOS-IT) : 2.16
Consensus Log Po/w : 1.69

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.61
Solubility : 0.619 mg/ml ; 0.00248 mol/l
Class : Soluble
Log S (Ali) : -1.78
Solubility : 4.14 mg/ml ; 0.0166 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.61
Solubility : 0.618 mg/ml ; 0.00247 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.68

Safety of [ 773869-57-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 773869-57-1 ]

* 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 [ 773869-57-1 ]
  • Downstream synthetic route of [ 773869-57-1 ]

[ 773869-57-1 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 58123-77-6 ]
  • [ 773869-57-1 ]
YieldReaction ConditionsOperation in experiment
88% With borane-THF In tetrahydrofuran at 60℃; for 2 h; Reference Example 14
5-(hydroxymethyl)-2-iodophenol
To a solution of 3-hydroxy-4-iodobenzoic acid (20.9 g, 79.3 mmol) in anhydrous THF (160 mL) was added 1 M borane THF solution (240 mL, 240 mmol) by small portions, and the mixture was stirred at 60°C for 2 hr.
Water was added to the reaction mixture, and the mixture was extracted twice with ethyl acetate.
The extract was washed with saturated brine, and dried over anhydrous sodium sulfate.
The solvent was evaporated under reduced pressure, and the residue was washed with diisopropyl ether and hexane to give the title compound (17.4 g, yield 88percent) as a white solid.
1H NMR (CDCl3) δ 1.69 (br, 1H), 4.64 (s, 2H), 5.33 (s, 1H), 6.70 (dd, J = 7.8, 1.5 Hz, 1H), 7.01 (d, J = 1.5 Hz, 1H), 7.63 (d, J = 7.8 Hz, 1H) .
Reference: [1] Patent: EP2351743, 2011, A1, . Location in patent: Page/Page column 117
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