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[ CAS No. 68043-53-8 ] {[proInfo.proName]}

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Chemical Structure| 68043-53-8
Chemical Structure| 68043-53-8
Structure of 68043-53-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 68043-53-8 ]

CAS No. :68043-53-8 MDL No. :MFCD04038185
Formula : C9H7NO4 Boiling Point : No data available
Linear Structure Formula :- InChI Key :KUAWMWVXZMQZLD-UHFFFAOYSA-N
M.W : 193.16 Pubchem ID :5228831
Synonyms :

Calculated chemistry of [ 68043-53-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 14
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.22
Num. rotatable bonds : 1
Num. H-bond acceptors : 4.0
Num. H-bond donors : 0.0
Molar Refractivity : 49.84
TPSA : 72.12 ?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) : -6.63 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.22
Log Po/w (XLOGP3) : 1.2
Log Po/w (WLOGP) : 1.56
Log Po/w (MLOGP) : -0.05
Log Po/w (SILICOS-IT) : 0.19
Consensus Log Po/w : 0.83

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.04
Solubility : 1.74 mg/ml ; 0.00902 mol/l
Class : Soluble
Log S (Ali) : -2.31
Solubility : 0.944 mg/ml ; 0.00489 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.24
Solubility : 1.11 mg/ml ; 0.00574 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 2.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.11

Safety of [ 68043-53-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 68043-53-8 ]

* 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 [ 68043-53-8 ]

[ 68043-53-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 80-65-9 ]
  • isopropyl alcohol hydrogen chloride [ No CAS ]
  • [ 68043-53-8 ]
  • [ 67863-82-5 ]
YieldReaction ConditionsOperation in experiment
107 g (88%) In nitromethane; benzene; EXAMPLE III 3-[(6-Nitro-4-chromanylidene)amino]-2-oxazolidinone An 85 g (0.44 mole) portion of 6-nitro-4-chromanone in 460 ml of benzene was treated with 1 ml of HCl (isopropanol) solution, using mechanical stirring, and refluxed until all water was removed via a Dean-Stark trap. The solution was then treated with 46 g (0.46 mole) of <strong>[80-65-9]3-amino-2-oxazolidinone</strong> and refluxed for 2.6 hr. A 7.9 ml portion of water was collected (theory: 7.9 ml). The reaction mixture was filtered hot, cooled to 10-11 for 3 hrs. and filtered. The orange crystalline solid was washed with 100 ml of benzene, ether and dried, m.p. 168-170. Yield: 107 g (88%). The product was recrystallized from 650 ml of nitromethane (Darco), washed with 100 ml of cold nitromethane, ether and dried, m.p. 170-171, Yield: 84 g (69%). Anal. Calcd. for C12 H11 N3 O5: C, 51.99; H, 4.00; N, 15.16. Found: C, 51.96; H, 4.03; N, 15.14.
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