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[ CAS No. 888504-28-7 ] Potassium 5-methyl-1,3,4-oxadiazole-2-carboxylate

Cat. No.: A138348
Chemical Structure| 888504-28-7
Chemical Structure| 888504-28-7
Structure of 888504-28-7 * Storage: Inert atmosphere,Store in freezer, under -20°C
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* Storage: Inert atmosphere,Store in freezer, under -20°C

* Shipping: Normal

Quality Control of [ 888504-28-7 ]

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Product Details of [ 888504-28-7 ]

CAS No. :888504-28-7 MDL No. :MFCD08060085
Formula : C4H3KN2O3 Boiling Point : -
Linear Structure Formula :- InChI Key :BRHMYHXNUGVBCU-UHFFFAOYSA-M
M.W : 166.18 Pubchem ID :24820502
Synonyms :

Calculated chemistry of [ 888504-28-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 10
Num. arom. heavy atoms : 5
Fraction Csp3 : 0.25
Num. rotatable bonds : 1
Num. H-bond acceptors : 5.0
Num. H-bond donors : 0.0
Molar Refractivity : 24.28
TPSA : 79.05 Ų

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) : -7.31 cm/s

Lipophilicity

Log Po/w (iLOGP) : -4.6
Log Po/w (XLOGP3) : 0.01
Log Po/w (WLOGP) : -1.26
Log Po/w (MLOGP) : -0.82
Log Po/w (SILICOS-IT) : 0.3
Consensus Log Po/w : -1.27

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.18
Solubility : 11.0 mg/ml ; 0.066 mol/l
Class : Very soluble
Log S (Ali) : -1.22
Solubility : 9.98 mg/ml ; 0.06 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -0.59
Solubility : 42.9 mg/ml ; 0.258 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 2.17

Safety of [ 888504-28-7 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 888504-28-7 ]

* 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 [ 888504-28-7 ]

[ 888504-28-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 518048-03-8 ]
  • [ 888504-28-7 ]
  • [ 518048-05-0 ]
YieldReaction ConditionsOperation in experiment
To a 0.5 liter reactor was added acetonitrile ( 15 vol), N-methylpyrrolidinone ( 1 vol) and N-methylmorpholine (0.5 g). The resulting solution was cooled to about 0C and then methyl oxadiazole- potassium (8g) was added. Pivaloyl chloride (7.22 ml) was then added dropwise (over 10 min). The resulting mixture was stirred for about 6 h.N-Methylmorpholine (5.9 g) and RLT-9 were then added. The resulting mixture was then heated to 20C and stirred for 16h. The solvent was then evaporated to provide a residue. Water (75 ml) and isopropyl alcohol (25 ml) were added to the residue. The resulting solution was stirred overnight at RT. A precipitate formed and was filtered and washed with water (10 ml) and IPA (20 ml). The product was dried under vacuum at 60C overnight to give 8.76g Raltegravir (85.7% assay, 77% yield). The obtained crude product was purified by slurry in MeOH/Water mixture.
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