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[ CAS No. 5398-69-6 ] {[proInfo.proName]}

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Chemical Structure| 5398-69-6
Chemical Structure| 5398-69-6
Structure of 5398-69-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 5398-69-6 ]

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Product Details of [ 5398-69-6 ]

CAS No. :5398-69-6 MDL No. :MFCD00277941
Formula : C7H4INO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :XWOGTRRVKVPJSP-UHFFFAOYSA-N
M.W : 293.02 Pubchem ID :220966
Synonyms :

Calculated chemistry of [ 5398-69-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 54.94
TPSA : 83.12 ?2

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) : -6.72 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.86
Log Po/w (XLOGP3) : 1.93
Log Po/w (WLOGP) : 1.9
Log Po/w (MLOGP) : 1.43
Log Po/w (SILICOS-IT) : 0.07
Consensus Log Po/w : 1.24

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 0.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -3.08
Solubility : 0.243 mg/ml ; 0.000828 mol/l
Class : Soluble
Log S (Ali) : -3.3
Solubility : 0.147 mg/ml ; 0.000502 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.09
Solubility : 2.36 mg/ml ; 0.00805 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 2.05

Safety of [ 5398-69-6 ]

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

Application In Synthesis of [ 5398-69-6 ]

* 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 [ 5398-69-6 ]

[ 5398-69-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 88-67-5 ]
  • [ 19230-50-3 ]
  • [ 5398-69-6 ]
YieldReaction ConditionsOperation in experiment
Synthesized according to a slight modification of two previously reported procedures.18 Neat2-iodobenzoic acid (3.00 g, 12.1 mmol) was cooled down to 0 C, to which was added a mixture offuming HNO3 (3.0 mL) and concentrated H2SO4 (13.5 mL). This mixture was then stirred at 0 C for 1 h,then at rt for 30 min, and finally at 135 C for 2 h, before being cooled back down to rt. The resultingsolution was poured into plenty of ice water and filtered. The solid was transferred to an Erlenmeyer flaskand suspended in water (300 mL), then heated to a boil. A solution of KI (2.41 g, 14.5 mmol) in water (15mL) acidified to pH 3 with a few drops of concentrated H2SO4 was added portion-wise to this boiling suspension (I2 vapors were generated with each portion). Omitting this step as in Subramanian?s reportyields the iodoso analog. The solution was filtered while still boiling, then the filtrate was stored at 4 Cfor 18 h after which time the desired compound precipitated. 2-Iodo-5-nitrobenzoic acid was thencollected by filtration while still cold to afford 1.73 g (49%) as a 13:2 mixture with the undesired2-iodo-3-nitrobenzoic acid isomer. The inseparable mixture was used as is in the next step.Characterization matches the data previously reported in the literature
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