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[ CAS No. 936-02-7 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 936-02-7
Chemical Structure| 936-02-7
Structure of 936-02-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 936-02-7 ]

CAS No. :936-02-7 MDL No. :MFCD00007599
Formula : C7H8N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :XSXYESVZDBAKKT-UHFFFAOYSA-N
M.W : 152.15 Pubchem ID :13637
Synonyms :

Calculated chemistry of [ 936-02-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 3.0
Molar Refractivity : 39.36
TPSA : 75.35 ?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) : -6.8 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.2
Log Po/w (XLOGP3) : 0.6
Log Po/w (WLOGP) : 0.0
Log Po/w (MLOGP) : 0.54
Log Po/w (SILICOS-IT) : -0.28
Consensus Log Po/w : 0.41

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.43
Solubility : 5.61 mg/ml ; 0.0369 mol/l
Class : Very soluble
Log S (Ali) : -1.76
Solubility : 2.67 mg/ml ; 0.0175 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.45
Solubility : 5.44 mg/ml ; 0.0357 mol/l
Class : Soluble

Medicinal Chemistry

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

Safety of [ 936-02-7 ]

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

Application In Synthesis of [ 936-02-7 ]

* 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 [ 936-02-7 ]

[ 936-02-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 32596-43-3 ]
  • [ 936-02-7 ]
  • [ 685528-17-0 ]
  • 2
  • [ 5555-00-0 ]
  • [ 936-02-7 ]
  • N'-(2-hydroxybenzoyl)-2-methylfuran-3-carbohydrazide [ No CAS ]
  • 3
  • [ 41042-12-0 ]
  • [ 936-02-7 ]
  • (E)-2-hydroxy-N'-(2-oxo-1-propylindolin-3-ylidene)benzohydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic acid; In methanol;Reflux; General procedure: Isatin based Schiff bases (1-20) were synthesized in three steps,first an esterification carried out by reacting different carboxylicacid with methanol in sulphuric acid (2-3 ml) under reflux conditionfor 12-16 h. The completion of reaction was monitored byTLC. After completion of reaction, reaction mixture was extractedwith hexane to obtained pure esters. Then esters were refluxedwith hydrazine hydrate in methanol with few drops of glacial aceticacid for 3 h. After completion of reaction, reaction mixture waswashed with chloroform to obtained different hydrazides. Thesehydrazides (1mmole) each were than treated with different Isatin(1mmole) in methanol having catalytic amount of glacial acetic acidfor 2-4 h. Reaction completion was monitored through periodicTLC. After completion of reaction, reaction mixture was washedwith n-hexane to obtain our desired products (1-20). The structureof all compounds was established through EI-MS and 1H NMR.
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