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[ CAS No. 99-56-9 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 99-56-9
Chemical Structure| 99-56-9
Structure of 99-56-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 99-56-9 ]

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Product Details of [ 99-56-9 ]

CAS No. :99-56-9 MDL No. :MFCD00007724
Formula : C6H7N3O2 Boiling Point : -
Linear Structure Formula :C6H3(NO2)(NH2)2 InChI Key :RAUWPNXIALNKQM-UHFFFAOYSA-N
M.W : 153.14 Pubchem ID :5111791
Synonyms :

Calculated chemistry of [ 99-56-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 2.0
Molar Refractivity : 44.07
TPSA : 97.86 ?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) : -6.61 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.69
Log Po/w (XLOGP3) : 0.88
Log Po/w (WLOGP) : 0.78
Log Po/w (MLOGP) : -0.3
Log Po/w (SILICOS-IT) : -1.73
Consensus Log Po/w : 0.06

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.68
Solubility : 3.19 mg/ml ; 0.0208 mol/l
Class : Very soluble
Log S (Ali) : -2.52
Solubility : 0.463 mg/ml ; 0.00302 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.04
Solubility : 13.8 mg/ml ; 0.0904 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.19

Safety of [ 99-56-9 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P301+P312+P330-P302+P352 UN#:N/A
Hazard Statements:H302-H317 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 99-56-9 ]

* 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 [ 99-56-9 ]
  • Downstream synthetic route of [ 99-56-9 ]

[ 99-56-9 ] Synthesis Path-Upstream   1~5

  • 1
  • [ 79-14-1 ]
  • [ 99-56-9 ]
  • [ 20034-00-8 ]
YieldReaction ConditionsOperation in experiment
87% at 130℃; for 3 h; General procedure: To a mixture of 1a–1c (10 mmol) with glycolic acid (2.28 g, 30 mmol) was added concentrated H3PO4(20 mL). The reaction mixture was refluxed at 130°C for 3 h, then quenched with 20percent NaOH. The respective solid product was collected by filtration.
Reference: [1] Russian Journal of General Chemistry, 2017, vol. 87, # 12, p. 3006 - 3016
[2] Bulletin of the Korean Chemical Society, 2013, vol. 34, # 4, p. 1272 - 1274
[3] Molecules, 2015, vol. 20, # 8, p. 15206 - 15223
[4] Journal of the American Chemical Society, 1952, vol. 74, p. 3689
[5] Journal of the American Chemical Society, 1957, vol. 79, p. 4391,4393
[6] Patent: US2004/209865, 2004, A1,
[7] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 2, p. 933 - 936
  • 2
  • [ 99-56-9 ]
  • [ 6295-06-3 ]
  • [ 89898-96-4 ]
  • [ 25652-34-0 ]
Reference: [1] Journal of the American Chemical Society, 1949, vol. 71, p. 6,7
  • 3
  • [ 924-44-7 ]
  • [ 99-56-9 ]
  • [ 89898-96-4 ]
  • [ 25652-34-0 ]
Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 21, p. 3153 - 3156
  • 4
  • [ 99-56-9 ]
  • [ 89898-96-4 ]
Reference: [1] Gazzetta Chimica Italiana, 1957, vol. 87, p. 354,365
  • 5
  • [ 99-56-9 ]
  • [ 6065-82-3 ]
  • [ 89898-96-4 ]
  • [ 25652-34-0 ]
Reference: [1] Justus Liebigs Annalen der Chemie, 1953, vol. 579, p. 212,220
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