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[ CAS No. 89102-73-8 ] {[proInfo.proName]}

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Chemical Structure| 89102-73-8
Chemical Structure| 89102-73-8
Structure of 89102-73-8 * Storage: {[proInfo.prStorage]}

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Product Details of [ 89102-73-8 ]

CAS No. :89102-73-8 MDL No. :MFCD07778413
Formula : C4H5NO2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :GBCAGXLDCTZCCT-UHFFFAOYSA-N
M.W : 99.09 Pubchem ID :12905096
Synonyms :

Calculated chemistry of [ 89102-73-8 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 22.63
TPSA : 46.26 ?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) : -7.25 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.08
Log Po/w (XLOGP3) : -0.48
Log Po/w (WLOGP) : 0.01
Log Po/w (MLOGP) : -0.94
Log Po/w (SILICOS-IT) : 0.77
Consensus Log Po/w : 0.09

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -0.61
Solubility : 24.1 mg/ml ; 0.243 mol/l
Class : Very soluble
Log S (Ali) : -0.02
Solubility : 93.6 mg/ml ; 0.945 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.99
Solubility : 10.2 mg/ml ; 0.103 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.16

Safety of [ 89102-73-8 ]

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 [ 89102-73-8 ]

* 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 [ 89102-73-8 ]

[ 89102-73-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 89102-73-8 ]
  • [ 57684-71-6 ]
YieldReaction ConditionsOperation in experiment
With triphenylphosphine; In tetrachloromethane; (b) 3-Chloromethyl isoxazole A solution of 3-hydroxymethyl isoxazole (4.23 g, 43 mmol) and triphenylphosphine (11.3 g, 42 mmol) in carbon tetrachloride (100 ml) was heated at reflux for 18 h. Solvent was removed under reduced pressure then the residue taken up in ether and filtered. The filtrate was concentrated under reduced pressure and further purified by short path distillation (bp 60 C. at 10 mm) to give the desired chloride (1.41 g, 12 mmol, 28%); deltaH (CDCl3) 4.50 (2H, s, CH2 --Cl), 6.40 (1H, d, J 2 Hz, CH-4), 8.40 (1H, d, J 2 Hz, CH-5).
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