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[ CAS No. 2113-51-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 2113-51-1
Chemical Structure| 2113-51-1
Structure of 2113-51-1 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 2113-51-1 ]

Related Doc. of [ 2113-51-1 ]

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Product Citations

Product Details of [ 2113-51-1 ]

CAS No. :2113-51-1 MDL No. :MFCD00039396
Formula : C12H9I Boiling Point : -
Linear Structure Formula :- InChI Key :QFUYDAGNUJWBSM-UHFFFAOYSA-N
M.W : 280.10 Pubchem ID :75025
Synonyms :
Chemical Name :2-Iodo-1,1'-biphenyl

Calculated chemistry of [ 2113-51-1 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 0.0
Num. H-bond donors : 0.0
Molar Refractivity : 64.6
TPSA : 0.0 ?2

Pharmacokinetics

GI absorption : Low
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.03 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.59
Log Po/w (XLOGP3) : 4.2
Log Po/w (WLOGP) : 3.96
Log Po/w (MLOGP) : 4.68
Log Po/w (SILICOS-IT) : 4.54
Consensus Log Po/w : 3.99

Druglikeness

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

Water Solubility

Log S (ESOL) : -4.84
Solubility : 0.00405 mg/ml ; 0.0000145 mol/l
Class : Moderately soluble
Log S (Ali) : -3.91
Solubility : 0.0345 mg/ml ; 0.000123 mol/l
Class : Soluble
Log S (SILICOS-IT) : -5.86
Solubility : 0.000386 mg/ml ; 0.00000138 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.04

Safety of [ 2113-51-1 ]

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

Application In Synthesis of [ 2113-51-1 ]

* 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 [ 2113-51-1 ]

[ 2113-51-1 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 626-44-8 ]
  • [ 2113-51-1 ]
  • [ 1165-57-7 ]
  • [ 5660-37-7 ]
  • [ 16322-10-4 ]
  • 3
  • [ 189999-35-7 ]
  • [ 99768-12-4 ]
  • [ 792-74-5 ]
  • [ 2113-51-1 ]
  • 4
  • [ 2113-51-1 ]
  • cyclohexyloxy(iodomethyl)dimethylsilane [ No CAS ]
  • [ 628692-15-9 ]
  • C26H32N2O2Si [ No CAS ]
  • 5
  • [ 1450-14-2 ]
  • [ 624-31-7 ]
  • [ 2113-51-1 ]
  • [ 3728-43-6 ]
  • [ 107384-77-0 ]
  • 6
  • [ 1450-14-2 ]
  • [ 624-31-7 ]
  • [ 2113-51-1 ]
  • [ 613-33-2 ]
  • [ 3728-43-6 ]
  • [ 107384-77-0 ]
  • 7
  • [ 2113-51-1 ]
  • [ 103962-05-6 ]
  • C19H11F3O [ No CAS ]
YieldReaction ConditionsOperation in experiment
49% With C22H14ClN3O2Pd; cesium acetate; sodium carbonate; In N,N-dimethyl-formamide; at 120℃; for 24h;Sealed tube; General procedure: A tubular reactor was charged with Na2CO3 (0.0424 g,0.4 mmol), CsOAc (0.1152 g, 0.6 mmol), 2-iodobiphenyl (0.0560 g,0.2 mmol), iodobenzene (0.0816 g, 0.4 mmol), A1 (10 at%), and solvent(3 mL), sealed, and heated to 120 C in an oil bath for 24 h.Subsequently, the reaction mixture was cooled and quenched withbrine (20 mL) and ethyl acetate (40 mL). The organic layer wasretained, and the aqueous phase was extracted with ethyl acetate(2 40 mL). All organic phases were combined, dried over anhydrousMgSO4, and filtered. The desired product was separated viavacuum distillation and was further purified by silica gel thin layerchromatography using petroleum ether as an expansion agent. Theproduct-containing silica gel was scraped off and pulverised. Thepowderwas leached with ethyl acetate for 4 h, and the leachatewasfiltered and subjected to vacuum distillation.
  • 8
  • [ 747392-34-3 ]
  • [ 2113-51-1 ]
  • 12-fluoro-9,10-dihydrotribenzo[b,d,f]azocine [ No CAS ]
  • 9
  • [ 2113-51-1 ]
  • [ 26118-14-9 ]
  • [ 68089-73-6 ]
  • 10
  • [ 2113-51-1 ]
  • [ 26767-16-8 ]
  • [ 68089-73-6 ]
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Technical Information

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