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[ CAS No. 1202-34-2 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1202-34-2
Chemical Structure| 1202-34-2
Structure of 1202-34-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 1202-34-2 ]

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Product Details of [ 1202-34-2 ]

CAS No. :1202-34-2 MDL No. :MFCD00006247
Formula : C10H9N3 Boiling Point : -
Linear Structure Formula :C5H4NNHNH4C5 InChI Key :HMMPCBAWTWYFLR-UHFFFAOYSA-N
M.W : 171.20 Pubchem ID :14547
Synonyms :
Chemical Name :Di(pyridin-2-yl)amine

Calculated chemistry of [ 1202-34-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 12
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 51.58
TPSA : 37.81 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.93 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.2
Log Po/w (XLOGP3) : 1.99
Log Po/w (WLOGP) : 2.22
Log Po/w (MLOGP) : 0.97
Log Po/w (SILICOS-IT) : 1.71
Consensus Log Po/w : 1.62

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.71
Solubility : 0.337 mg/ml ; 0.00197 mol/l
Class : Soluble
Log S (Ali) : -2.41
Solubility : 0.666 mg/ml ; 0.00389 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.21
Solubility : 0.0104 mg/ml ; 0.000061 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.07

Safety of [ 1202-34-2 ]

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 [ 1202-34-2 ]

* 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 [ 1202-34-2 ]

[ 1202-34-2 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 5027-32-7 ]
  • [ 1202-34-2 ]
  • [ 6147-53-1 ]
  • (((CH3CO)2CH)2)4Co4((C5H4N)2NH)4 [ No CAS ]
  • 3Co(2+)*4CH3COO(1-)*2(C5H4N)2NH(1-)=Co3(O2CCH3)4((C5H4N)NH(C5H4N))2 [ No CAS ]
  • 2
  • [ 5027-32-7 ]
  • [ 1202-34-2 ]
  • copper(II) trifluoroacetate [ No CAS ]
  • [ 245483-57-2 ]
  • 3
  • [ 5027-32-7 ]
  • [ 1202-34-2 ]
  • [ 6147-53-1 ]
  • [Co(C10H12O4)(2,2'-dipyridylamine)4](CH3CO2)2(H2O)2/CH3OH [ No CAS ]
  • 4
  • [ 1202-34-2 ]
  • [ 4181-20-8 ]
  • [ 147970-27-2 ]
  • 5
  • [ 1202-34-2 ]
  • cobalt(II) chloride hexahydrate [ No CAS ]
  • [ 42835-25-6 ]
  • C38H31CoF2N5O6*H2O [ No CAS ]
  • 6
  • [ 1202-34-2 ]
  • manganese(II) chloride tetrahydrate [ No CAS ]
  • [ 42835-25-6 ]
  • Mn(flmq)2(2,2′-bipyridylamine) [ No CAS ]
YieldReaction ConditionsOperation in experiment
60% General procedure: The methanolic solution (15mL) containing <strong>[42835-25-6]flumequine</strong> (0.4mmol, 104mg) and KOH (0.4mmol, 22mg) was added, after a 30-min stirring, slowly and simultaneously with a methanolic solution of phen (0.2mmol, 36mg) to a methanolic solution (10mL) of MnCl2·4H2O (0.2mmol, 40mg). The resultant solution was stirred for 15min and left for slow evaporation. Yellow crystals of [Mn(flmq)2(phen)], 2 (98mg, yield: 65%) suitable for X-ray structure determination, were collected after a few days.
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