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[ CAS No. 21883-13-6 ] {[proInfo.proName]}

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Chemical Structure| 21883-13-6
Chemical Structure| 21883-13-6
Structure of 21883-13-6 * Storage: {[proInfo.prStorage]}

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Product Details of [ 21883-13-6 ]

CAS No. :21883-13-6 MDL No. :MFCD03425692
Formula : C9H9NO Boiling Point : -
Linear Structure Formula :- InChI Key :PXAQQUKODRZAOZ-UHFFFAOYSA-N
M.W : 147.17 Pubchem ID :3801022
Synonyms :

Calculated chemistry of [ 21883-13-6 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 1
Num. H-bond acceptors : 2.0
Num. H-bond donors : 0.0
Molar Refractivity : 42.62
TPSA : 33.02 ?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) : -6.04 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.09
Log Po/w (XLOGP3) : 1.63
Log Po/w (WLOGP) : 1.88
Log Po/w (MLOGP) : 1.44
Log Po/w (SILICOS-IT) : 2.26
Consensus Log Po/w : 1.86

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.12
Solubility : 1.12 mg/ml ; 0.00764 mol/l
Class : Soluble
Log S (Ali) : -1.94
Solubility : 1.71 mg/ml ; 0.0116 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.98
Solubility : 0.155 mg/ml ; 0.00105 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.35

Safety of [ 21883-13-6 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P280-P305+P351+P338-P310 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 21883-13-6 ]

* 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 [ 21883-13-6 ]

[ 21883-13-6 ] Synthesis Path-Downstream   1~5

  • 2
  • [ 27060-75-9 ]
  • [ 557-21-1 ]
  • [ 21883-13-6 ]
  • 3
  • [ 21883-13-6 ]
  • [ 86-81-7 ]
  • 6-amino-2,9-dimethoxy-11,12-dihydro-11-(3,4,5-trimethoxyphenyl)benzo[c]phenanthridine [ No CAS ]
  • 4
  • [ 21883-13-6 ]
  • 6-amino-2,9-dimethoxy-11-(3,4,5-trimethoxyphenyl)benzo[c]phenanthridine [ No CAS ]
  • 5
  • [ 924-88-9 ]
  • [ 21883-13-6 ]
  • 3,6-Bis(2'-methyl-4'-methoxyphenyl)-2,5-dihydropyrrolo(3,4-c)-pyrrole-1,4-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.82 g (3.86%) With potassium tert-butylate; In tert-Amyl alcohol; EXAMPLE 12 3,6-Bis(2'-methyl-4'-methoxyphenyl)-2,5-dihydropyrrolo(3,4-c)-pyrrole-1,4-dione 36.79 g (250 mmol) of <strong>[21883-13-6]2-methyl-4-methoxybenzonitrile</strong> and 28.05 g of potassium tert-butylate in 60 ml of tert-amyl alcohol are reacted with 25.28 g (125 mmol) of diisopropyl succinate in 10 ml of tert-amyl alcohol. Yield 1.82 g (3.86%) of orange powder. Purification is carried out by extractive recrystallisation from toluene by the process described by H. Langhals in Chem. Ber. 118, (1985), 4641. Melting point 319 C. (dec.).=Rf (silica gel/CHCl3)=0.17. UV(DMSO): lambdamax (1 g epsilon)=460 nm (4,405). Fluorescence (DMSO): lambdamax =519 nm. C22 H20 N2 O4 (376.39) Calc.: C, 70.20; H, 5.35; N, 7.44. Found: C, 70.20; H, 5.46; N, 7.24.
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