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[ CAS No. 3922-40-5 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 3922-40-5
Chemical Structure| 3922-40-5
Structure of 3922-40-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 3922-40-5 ]

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Product Details of [ 3922-40-5 ]

CAS No. :3922-40-5 MDL No. :MFCD00004975
Formula : C12H8N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :SLIBCJURSADKPV-UHFFFAOYSA-N
M.W : 212.20 Pubchem ID :77524
Synonyms :

Calculated chemistry of [ 3922-40-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 16
Num. arom. heavy atoms : 14
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 4.0
Num. H-bond donors : 2.0
Molar Refractivity : 61.09
TPSA : 66.24 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : Yes
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : Yes
CYP3A4 inhibitor : Yes
Log Kp (skin permeation) : -6.35 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.89
Log Po/w (XLOGP3) : 1.75
Log Po/w (WLOGP) : 2.19
Log Po/w (MLOGP) : 0.67
Log Po/w (SILICOS-IT) : 1.95
Consensus Log Po/w : 1.49

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.91
Solubility : 0.264 mg/ml ; 0.00124 mol/l
Class : Soluble
Log S (Ali) : -2.76
Solubility : 0.37 mg/ml ; 0.00174 mol/l
Class : Soluble
Log S (SILICOS-IT) : -3.86
Solubility : 0.0292 mg/ml ; 0.000138 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.53

Safety of [ 3922-40-5 ]

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

Application In Synthesis of [ 3922-40-5 ]

* 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 [ 3922-40-5 ]
  • Downstream synthetic route of [ 3922-40-5 ]

[ 3922-40-5 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 3922-40-5 ]
  • [ 156492-30-7 ]
YieldReaction ConditionsOperation in experiment
25% at 110℃; for 8 h; Inert atmosphere 4,7-Dihydroxy-1,10-phenanthroline (380mg, 1.80mmol), PBr3 (530mg, 1.96mmol) and POBr3 (2.4g, 8.4mmol)were heated at 110°C for 8h under Ar-gas atmosphere. Afterthe reaction, ice (ca. 100g) was poured into the mixture and thesolution pH was adjusted to 8 with an aqueous 10percent NaOH solution. The mixture was then extracted with CH2Cl2 (100mL) three times. The combined organic phase was dried overanhydrous MgSO4 and evaporated to dryness under reducedpressure. The resulting products were purified by columnchromatography (SiO2, CHCl3), affording pure 4,7-Br2-phen(151mg, 25percent). Rf = 0.40 (SiO2, CHCl3). 1HNMR (270MHz,CDCl3): δ/ppm 7.97 (d, 2H, J = 4.8Hz, 3,8-Ar-H), 8.33(s, 2H, 5,6-Ar-H), 8.95 (d, 2H, J = 4.8Hz, 2,9-Ar-H). ESI-MSm/z 339 ([M+H]+).
Reference: [1] European Journal of Inorganic Chemistry, 2017, vol. 2017, # 32, p. 3794 - 3798
[2] Bulletin of the Chemical Society of Japan, 2017, vol. 90, # 5, p. 574 - 585
  • 2
  • [ 3922-40-5 ]
  • [ 156492-30-7 ]
Reference: [1] Synlett, 1997, vol. 1997, # 6, p. 710 - 712
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[ 3922-40-5 ]

Chemical Structure| 61626-11-7

A101578[ 61626-11-7 ]

1,10-Phenanthroline-4,7-diol hydrochloride

Reason: Free-Salt

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