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[ CAS No. 2578-45-2 ] {[proInfo.proName]}

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Chemical Structure| 2578-45-2
Chemical Structure| 2578-45-2
Structure of 2578-45-2 * Storage: {[proInfo.prStorage]}

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Product Details of [ 2578-45-2 ]

CAS No. :2578-45-2 MDL No. :MFCD00006233
Formula : C5H2ClN3O4 Boiling Point : -
Linear Structure Formula :- InChI Key :QLHVJBXAQWPEDI-UHFFFAOYSA-N
M.W : 203.54 Pubchem ID :75738
Synonyms :

Calculated chemistry of [ 2578-45-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 13
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 46.89
TPSA : 104.53 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.5 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.31
Log Po/w (XLOGP3) : 1.47
Log Po/w (WLOGP) : 1.55
Log Po/w (MLOGP) : -0.3
Log Po/w (SILICOS-IT) : -2.11
Consensus Log Po/w : 0.19

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.24
Solubility : 1.18 mg/ml ; 0.00579 mol/l
Class : Soluble
Log S (Ali) : -3.27
Solubility : 0.109 mg/ml ; 0.000535 mol/l
Class : Soluble
Log S (SILICOS-IT) : -1.41
Solubility : 7.96 mg/ml ; 0.0391 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 3.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.32

Safety of [ 2578-45-2 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P264-P270-P280-P301+P310+P330-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:2811
Hazard Statements:H300-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2578-45-2 ]

* 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.

  • Upstream synthesis route of [ 2578-45-2 ]
  • Downstream synthetic route of [ 2578-45-2 ]

[ 2578-45-2 ] Synthesis Path-Upstream   1~3

  • 1
  • [ 2578-45-2 ]
  • [ 4318-78-9 ]
YieldReaction ConditionsOperation in experiment
85% With hydrogen In ethanol at 25℃; for 18 h; 2-Chloro-3,5-dinitropyridine (4.98 g, 24.46 mmol) was dissolved in ethanol (500 mL) and 5percent palladium on carbon (3.74 g, 0.75 g/g substrate) was added. The mixture was hydrogenated at 25° C. under 50 psi of hydrogen for 18 hrs. The mixture was filtered through celite to remove the catalyst and concentrated under reduced pressure. Purification (silica gel, 20:2:1 CHCl3/MeOH/NH4OH, followed by 12:2:1 CHCl3/MeOH/NH4OH) gave 3,5-diaminopyridine (2.27 g, 85percent) as a brown solid. 1H (CD3OD) δ 7.32 (d, 2H, J=2 Hz), 6.45-6.43 (m, 1H).
Reference: [1] Patent: US6750348, 2004, B1, . Location in patent: Page column 113
[2] Recueil des Travaux Chimiques des Pays-Bas, 1953, vol. 72, p. 569,573
[3] Recueil des Travaux Chimiques des Pays-Bas, 1953, vol. 72, p. 569,573
[4] Recueil des Travaux Chimiques des Pays-Bas, 1953, vol. 72, p. 569,573
[5] Patent: US5668157, 1997, A,
  • 2
  • [ 2578-45-2 ]
  • [ 5632-81-5 ]
Reference: [1] ChemBioChem, 2010, vol. 11, # 10, p. 1364-1367+1315
[2] Patent: US5668157, 1997, A,
  • 3
  • [ 2578-45-2 ]
  • [ 7439-89-6 ]
  • [ 5632-81-5 ]
Reference: [1] Patent: US5998436, 1999, A,
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