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[ CAS No. 72792-54-2 ]

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Chemical Structure| 72792-54-2
Chemical Structure| 72792-54-2
Structure of 72792-54-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 72792-54-2 ]

CAS No. :72792-54-2 MDL No. :MFCD01438626
Formula : C3H6ClN3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W :151.62 Pubchem ID :-
Synonyms :

Calculated chemistry of [ 72792-54-2 ]

Physicochemical Properties

Num. heavy atoms : 8
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 1.0
Num. H-bond donors : 2.0
Molar Refractivity : 37.89
TPSA : 93.17 Ų

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) : -6.47 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.0
Log Po/w (XLOGP3) : 1.06
Log Po/w (WLOGP) : 1.13
Log Po/w (MLOGP) : -0.41
Log Po/w (SILICOS-IT) : 0.95
Consensus Log Po/w : 0.54

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -1.91
Solubility : 1.86 mg/ml ; 0.0123 mol/l
Class : Very soluble
Log S (Ali) : -2.61
Solubility : 0.374 mg/ml ; 0.00247 mol/l
Class : Soluble
Log S (SILICOS-IT) : -0.52
Solubility : 45.8 mg/ml ; 0.302 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.39

Safety of [ 72792-54-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 72792-54-2 ]

* 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 [ 72792-54-2 ]

[ 72792-54-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 72792-54-2 ]
  • [ 108-24-7 ]
  • [ 56503-71-0 ]
  • 2
  • [ 1447226-47-2 ]
  • [ 72792-54-2 ]
  • N-(2-aminothiazol-4-yl)-6-chloro-4-(isopropylamino)nicotinamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20.0℃; for 1.0h; A mixture of 6-chloro-4-(isopropylamino)nicotinic acid (0.15 g, 0.70 mmol), 2,4-diamino thiazole hydrochloride (0.21 g, 1.4 mmol), 1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (0.32 g, 0.84 mmol) and N,N-diisopropylethylamine (0.40 ml, 2.3 mmol) in 20 mL DMF was stirred at room temperature for 1 hour. Water was added, and the product was extracted into ethyl acetate. The ethyl acetate solution was concentrated under reduced pressure.
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