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[ CAS No. 24415-66-5 ] {[proInfo.proName]}

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Chemical Structure| 24415-66-5
Chemical Structure| 24415-66-5
Structure of 24415-66-5 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 24415-66-5 ]

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Product Details of [ 24415-66-5 ]

CAS No. :24415-66-5 MDL No. :MFCD00227619
Formula : C6H5ClN4 Boiling Point : No data available
Linear Structure Formula :(CH3)C5H2N4Cl InChI Key :NOIPEBKPGPZXNR-UHFFFAOYSA-N
M.W : 168.58 Pubchem ID :520127
Synonyms :

Calculated chemistry of [ 24415-66-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.17
Num. rotatable bonds : 0
Num. H-bond acceptors : 3.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.76
TPSA : 43.08 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.29 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.65
Log Po/w (XLOGP3) : 1.46
Log Po/w (WLOGP) : 1.09
Log Po/w (MLOGP) : 1.14
Log Po/w (SILICOS-IT) : 1.08
Consensus Log Po/w : 1.28

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.41
Solubility : 0.655 mg/ml ; 0.00389 mol/l
Class : Soluble
Log S (Ali) : -1.97
Solubility : 1.8 mg/ml ; 0.0107 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.34
Solubility : 0.776 mg/ml ; 0.0046 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.97

Safety of [ 24415-66-5 ]

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 [ 24415-66-5 ]

* 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 [ 24415-66-5 ]

[ 24415-66-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 7343-33-1 ]
  • [ 24415-66-5 ]
  • 7-(3-bromo-[1,2,4]triazol-1-yl)-5-methyl-[1,2,4]triazolo[1,5-<i>a</i>]pyrimidine [ No CAS ]
  • 2
  • [ 24415-66-5 ]
  • [ 131395-17-0 ]
  • [ 1281860-82-9 ]
  • 3
  • [ 24415-66-5 ]
  • [ 16803-92-2 ]
  • N-(4-chlorophenyl)-4-((5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-yl)amino)benzenesulfonamide hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
98% General procedure: A mixture of 0.001 mol of compound (41a-d or 45), 1 equivalentof the respective 4-amino-N-arylbenzenesulfonamides (44a-g) and3 mL of ethanol was stirred and refluxed (78 C) for 2 h. The reactionmixture was poured into ice water, and the precipitateformed was vacuum filtered and washed with water. The precipitatewas purified by recrystallization from methanol/water (2:1) orchromatography TLC Glass Plates (Merck TLC Silica gel 60 RP-18F254s) in chloroform/methanol (9.5:0.5). After purification, therespective hydrochloride was prepared, and the molecules weresolubilized and stirred for 15 min in a 1:1 solution of HCl/H2O andconcentrated under vacuum [17e19].
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