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[ CAS No. 55984-93-5 ] {[proInfo.proName]}

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Chemical Structure| 55984-93-5
Chemical Structure| 55984-93-5
Structure of 55984-93-5 * Storage: {[proInfo.prStorage]}

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Product Details of [ 55984-93-5 ]

CAS No. :55984-93-5 MDL No. :MFCD00119249
Formula : C9H6N2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :UJXAVMZSVIODSH-UHFFFAOYSA-N
M.W : 142.16 Pubchem ID :10419286
Synonyms :

Calculated chemistry of [ 55984-93-5 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.11
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 40.84
TPSA : 47.58 ?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 : Yes
Log Kp (skin permeation) : -5.95 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.72
Log Po/w (XLOGP3) : 1.72
Log Po/w (WLOGP) : 1.74
Log Po/w (MLOGP) : 1.08
Log Po/w (SILICOS-IT) : 2.24
Consensus Log Po/w : 1.7

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.21
Solubility : 0.879 mg/ml ; 0.00619 mol/l
Class : Soluble
Log S (Ali) : -2.34
Solubility : 0.657 mg/ml ; 0.00462 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.93
Solubility : 0.167 mg/ml ; 0.00117 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.34

Safety of [ 55984-93-5 ]

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

Application In Synthesis of [ 55984-93-5 ]

* 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 [ 55984-93-5 ]

[ 55984-93-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 615-59-8 ]
  • [ 55984-93-5 ]
  • 2
  • [ 55984-93-5 ]
  • [ 5156-01-4 ]
YieldReaction ConditionsOperation in experiment
58% 2) The <strong>[55984-93-5]2-<strong>[55984-93-5]methylterephthalonitrile</strong></strong> thus obtained is then added to 70 ml of 95percent H2SO4, the mixture is maintained at 100° C. overnight, and after stopping the heating, 35 ml of H2O are added thereto and, once at room temperature, 6.6 g of NaNO2 dissolved in 30 ml of H2O are added. The whole is maintained at 110° C. overnight. Finally, after adding 200 ml of H2O with stirring, filtering through a Buechner funnel, washing with water and drying under vacuum at 50° C. overnight, 2.13 g of 2-methylterephthalic acid are obtained in the form of a whitish powder (Yield of 58percent).
  • 3
  • [ 623-26-7 ]
  • [ 98689-31-7 ]
  • [ 55984-93-5 ]
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