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[ CAS No. 17302-46-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 17302-46-4
Chemical Structure| 17302-46-4
Structure of 17302-46-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 17302-46-4 ]

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Product Details of [ 17302-46-4 ]

CAS No. :17302-46-4 MDL No. :MFCD00024695
Formula : C8H7NO5 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UUBFELFUKFJSRD-UHFFFAOYSA-N
M.W : 197.15 Pubchem ID :87041
Synonyms :

Calculated chemistry of [ 17302-46-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 5.0
Num. H-bond donors : 1.0
Molar Refractivity : 48.57
TPSA : 92.35 ?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) : -5.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.56
Log Po/w (XLOGP3) : 2.67
Log Po/w (WLOGP) : 1.09
Log Po/w (MLOGP) : 0.3
Log Po/w (SILICOS-IT) : -0.9
Consensus Log Po/w : 0.94

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.86
Solubility : 0.27 mg/ml ; 0.00137 mol/l
Class : Soluble
Log S (Ali) : -4.26
Solubility : 0.0108 mg/ml ; 0.0000548 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -1.28
Solubility : 10.3 mg/ml ; 0.052 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.87

Safety of [ 17302-46-4 ]

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

Application In Synthesis of [ 17302-46-4 ]

* 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 [ 17302-46-4 ]

[ 17302-46-4 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 67-56-1 ]
  • [ 17302-46-4 ]
  • [ 22802-67-1 ]
YieldReaction ConditionsOperation in experiment
600 mg With palladium 10% on activated carbon; hydrogen; sodium sulfate; under 2585.81 Torr; The hydrogenation of methyl 2-hydroxy-5-nitrobenzoate (700 mg, 3.3 mmol) using 10% Pd-C (100 mg) and Na2SO4 (100 mg) in MeOH at 50 psi gave methyl 5-amino-2-methoxybenzoate (600 mg).
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