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[ CAS No. 354512-22-4 ] {[proInfo.proName]}

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Chemical Structure| 354512-22-4
Chemical Structure| 354512-22-4
Structure of 354512-22-4 * Storage: {[proInfo.prStorage]}

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Product Details of [ 354512-22-4 ]

CAS No. :354512-22-4 MDL No. :MFCD09038015
Formula : C8H7NO4 Boiling Point : -
Linear Structure Formula :- InChI Key :XZFQLZGPDRXXHV-UHFFFAOYSA-N
M.W : 181.15 Pubchem ID :12137088
Synonyms :

Calculated chemistry of [ 354512-22-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 3
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 47.14
TPSA : 72.12 ?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) : -6.57 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.24
Log Po/w (XLOGP3) : 1.18
Log Po/w (WLOGP) : 1.42
Log Po/w (MLOGP) : 0.03
Log Po/w (SILICOS-IT) : -0.17
Consensus Log Po/w : 0.74

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.85
Solubility : 2.56 mg/ml ; 0.0141 mol/l
Class : Very soluble
Log S (Ali) : -2.29
Solubility : 0.929 mg/ml ; 0.00513 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.85
Solubility : 2.54 mg/ml ; 0.014 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.98

Safety of [ 354512-22-4 ]

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

Application In Synthesis of [ 354512-22-4 ]

* 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.

  • Upstream synthesis route of [ 354512-22-4 ]

[ 354512-22-4 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 354525-36-3 ]
  • [ 354512-22-4 ]
YieldReaction ConditionsOperation in experiment
76% With dipyridinium dichromate In dichloromethane at 10 - 20℃; for 3 h; [0095] Step 3. To a solution of (3-methoxy-5-nitrophenyl)methanol (75 g, 0.41 mol) in CH2C12 (1.5 L) was added pyridinium dichromate (382 g, 1.02 mol) and silica gel (382 g) below 10 °C. After stirring at room temperature for 3 h, TLC analysis showed the starting material was consumed completely (3: 1 petroleum/ethyl acetate, Rf 0.6). The mixture was purified by flash column chromatography using CH2C12 to afford 3-methoxy-5-nitrobenzaldehyde as a yellow solid (170 g, 76percent, 3 batches).
Reference: [1] Patent: WO2013/148365, 2013, A1, . Location in patent: Paragraph 0095
[2] Journal of Medicinal Chemistry, 2004, vol. 47, # 11, p. 2897 - 2905
[3] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304
  • 2
  • [ 78238-13-8 ]
  • [ 354512-22-4 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2011, vol. 2, # 10, p. 735 - 740
[2] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304
  • 3
  • [ 99-34-3 ]
  • [ 354512-22-4 ]
Reference: [1] Journal of Medicinal Chemistry, 2004, vol. 47, # 11, p. 2897 - 2905
[2] Patent: WO2013/148365, 2013, A1,
[3] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304
  • 4
  • [ 78238-12-7 ]
  • [ 354512-22-4 ]
Reference: [1] Journal of Medicinal Chemistry, 2004, vol. 47, # 11, p. 2897 - 2905
[2] Patent: WO2013/148365, 2013, A1,
[3] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304
  • 5
  • [ 2702-58-1 ]
  • [ 354512-22-4 ]
Reference: [1] ACS Medicinal Chemistry Letters, 2011, vol. 2, # 10, p. 735 - 740
[2] MedChemComm, 2018, vol. 9, # 8, p. 1293 - 1304
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