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[ CAS No. 33631-02-6 ] {[proInfo.proName]}

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Chemical Structure| 33631-02-6
Chemical Structure| 33631-02-6
Structure of 33631-02-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 33631-02-6 ]

CAS No. :33631-02-6 MDL No. :MFCD10000606
Formula : C5H7N3O Boiling Point : -
Linear Structure Formula :- InChI Key :BHTKBUHNIZPKSG-UHFFFAOYSA-N
M.W : 125.13 Pubchem ID :23423669
Synonyms :

Calculated chemistry of [ 33631-02-6 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 3.0
Molar Refractivity : 35.07
TPSA : 85.16 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.44 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.1
Log Po/w (XLOGP3) : -0.53
Log Po/w (WLOGP) : -0.03
Log Po/w (MLOGP) : -1.03
Log Po/w (SILICOS-IT) : -0.49
Consensus Log Po/w : -0.4

Druglikeness

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

Water Solubility

Log S (ESOL) : -0.78
Solubility : 21.0 mg/ml ; 0.168 mol/l
Class : Very soluble
Log S (Ali) : -0.79
Solubility : 20.3 mg/ml ; 0.162 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.69
Solubility : 25.6 mg/ml ; 0.205 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.67

Safety of [ 33631-02-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 33631-02-6 ]

* 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 [ 33631-02-6 ]
  • Downstream synthetic route of [ 33631-02-6 ]

[ 33631-02-6 ] Synthesis Path-Upstream   1~7

  • 1
  • [ 33631-02-6 ]
  • [ 272-97-9 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
  • 2
  • [ 33631-02-6 ]
  • [ 2770-01-6 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
  • 3
  • [ 3243-24-1 ]
  • [ 33631-02-6 ]
  • [ 2770-01-6 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
  • 4
  • [ 33631-02-6 ]
  • [ 64-18-6 ]
  • [ 3243-24-1 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
  • 5
  • [ 88511-57-3 ]
  • [ 33631-02-6 ]
YieldReaction ConditionsOperation in experiment
83% With hydrogen In DMF (N,N-dimethyl-formamide) at 20℃; 3d)
3,4-diamino-2-hydroxypyridine
11.0 g (71 mmol) of 4-amino-2-hydroxy-3-nitropyridine were dissolved in 150 ml of dimethylformamide and reduced by catalytic hydrogenation at ambient temperature (Pd/C 10percent).
Yield: 83percent of theory. C5H7N3O (125.13) Mass spectrum: (M+H)+=126
Reference: [1] Patent: US2005/20574, 2005, A1, . Location in patent: Page/Page column 16
  • 6
  • [ 1681-37-4 ]
  • [ 33631-02-6 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
  • 7
  • [ 3243-24-1 ]
  • [ 33631-02-6 ]
  • [ 2770-01-6 ]
Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1949, vol. 68, p. 1013,1024
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