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[ CAS No. 704-14-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 704-14-3
Chemical Structure| 704-14-3
Structure of 704-14-3 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 704-14-3 ]

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Product Details of [ 704-14-3 ]

CAS No. :704-14-3 MDL No. :MFCD00100932
Formula : C7H7NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :NRTULWPODYLFOJ-UHFFFAOYSA-N
M.W : 169.14 Pubchem ID :219635
Synonyms :

Calculated chemistry of [ 704-14-3 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.14
Num. rotatable bonds : 2
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 43.78
TPSA : 75.28 ?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) : -5.9 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.99
Log Po/w (XLOGP3) : 2.02
Log Po/w (WLOGP) : 1.31
Log Po/w (MLOGP) : 0.05
Log Po/w (SILICOS-IT) : -0.8
Consensus Log Po/w : 0.71

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.4
Solubility : 0.675 mg/ml ; 0.00399 mol/l
Class : Soluble
Log S (Ali) : -3.23
Solubility : 0.1 mg/ml ; 0.000591 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.32
Solubility : 8.0 mg/ml ; 0.0473 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.79

Safety of [ 704-14-3 ]

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

Application In Synthesis of [ 704-14-3 ]

* 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.

  • Downstream synthetic route of [ 704-14-3 ]

[ 704-14-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 150-19-6 ]
  • [ 3114-61-2 ]
  • [ 16292-95-8 ]
  • [ 704-14-3 ]
YieldReaction ConditionsOperation in experiment
4.7%; 34%; 29% With bismuth (III) nitrate pentahydrate; In acetone; at 0℃; for 20.0h; General procedure: To a solid mixture of phenol (1-3 equiv) and Bi(NO3)35H2O (1 equiv) or Fe(NO3)39H2O (1 equiv) was added acetone (10 ml/mmol). The resulting mixture was stirred at room temperature under air or at reflux for 2-24 hours, Tables 1 and 2. When the reaction was completed the insoluble materials were filtered off using a pad of Celite and the residue was washed by acetone (ca. 5 ml/mmol). The filtrate was treated by NaHCO3 (0.1 g/mmol) until evolution of CO2 stopped. Insoluble material was filtered off again, and the solvent was removed under vacuum in a water bath 25-35C. The nitrated products were separated or purified using silica gel chromatography, to give pure phenolic compounds. All products were characterized by 1H NMR,13C NMR and IR and were identified by comparison of the spectral data and melting points with those reported in literature and characterized.
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