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[ CAS No. 39745-39-6 ] {[proInfo.proName]}

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Chemical Structure| 39745-39-6
Chemical Structure| 39745-39-6
Structure of 39745-39-6 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 39745-39-6 ]

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Product Details of [ 39745-39-6 ]

CAS No. :39745-39-6 MDL No. :MFCD03001414
Formula : C6H6N2O3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :YVYDGIGILRUPED-UHFFFAOYSA-N
M.W : 154.12 Pubchem ID :543029
Synonyms :

Calculated chemistry of [ 39745-39-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.17
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 1.0
Molar Refractivity : 40.05
TPSA : 78.94 ?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) : -6.1 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.1
Log Po/w (XLOGP3) : 1.61
Log Po/w (WLOGP) : 1.0
Log Po/w (MLOGP) : -0.56
Log Po/w (SILICOS-IT) : -0.81
Consensus Log Po/w : 0.47

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.15
Solubility : 1.1 mg/ml ; 0.00712 mol/l
Class : Soluble
Log S (Ali) : -2.88
Solubility : 0.203 mg/ml ; 0.00132 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.2
Solubility : 9.66 mg/ml ; 0.0627 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.85

Safety of [ 39745-39-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 39745-39-6 ]

* 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 [ 39745-39-6 ]
  • Downstream synthetic route of [ 39745-39-6 ]

[ 39745-39-6 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 21901-29-1 ]
  • [ 39745-39-6 ]
YieldReaction ConditionsOperation in experiment
77% at 0℃; for 16 h; Synthesis of the compound 25 The compound 24 (10g, 0.065 mol) was added into 100 mL of water, a concentrated sulphuric acid (12 mL) was slowly added with agitation and cooled to 0 °C in an ice bath. Sodium nitrite (6.9 g, 0.098 mol) was added in batches, reacted at 0°C for 4h, and left standing for 12 h. A large amount of yellow precipitate was precipitated, filtrated under the reduced pressure, vacuum-dried to obtain 7.7 g of a yellow product with a yield of 77percent. The melting point is 216.5-218.5°C (water).
Reference: [1] Patent: EP2366691, 2011, A1, . Location in patent: Page/Page column 11
[2] Journal of the American Chemical Society, 1952, vol. 74, p. 3828,3830
  • 2
  • [ 14011-21-3 ]
  • [ 41125-09-1 ]
  • [ 39745-39-6 ]
Reference: [1] Journal of Medicinal Chemistry, 2000, vol. 43, # 22, p. 4288 - 4312
  • 3
  • [ 21901-29-1 ]
  • [ 39745-39-6 ]
  • [ 56057-19-3 ]
Reference: [1] Journal of the American Chemical Society, 1947, vol. 69, p. 63,66
[2] Journal of Heterocyclic Chemistry, 1996, vol. 33, # 6, p. 1815 - 1821
[3] Journal of the American Chemical Society, 1947, vol. 69, p. 63,66
[4] Journal of Heterocyclic Chemistry, 1996, vol. 33, # 6, p. 1815 - 1821
  • 4
  • [ 1824-81-3 ]
  • [ 39745-39-6 ]
Reference: [1] Journal of the American Chemical Society, 1947, vol. 69, p. 63,66
[2] Patent: EP2366691, 2011, A1,
  • 5
  • [ 109-06-8 ]
  • [ 39745-39-6 ]
Reference: [1] Journal of the American Chemical Society, 1947, vol. 69, p. 63,66
  • 6
  • [ 56057-19-3 ]
  • [ 21203-68-9 ]
  • [ 39745-39-6 ]
Reference: [1] Journal of the American Chemical Society, 1954, vol. 76, p. 596,598
  • 7
  • [ 70959-85-2 ]
  • [ 39745-39-6 ]
  • [ 39073-14-8 ]
Reference: [1] Journal of Heterocyclic Chemistry, 1996, vol. 33, # 6, p. 1815 - 1821
  • 8
  • [ 3279-76-3 ]
  • [ 39745-39-6 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
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