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51517-09-0,MFCD19673344
Catalog No.:AA00J2HH

51517-09-0 | 1,3,4-Oxadiazol-2-ol

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100mg
95%
in stock  
$77.00   $54.00
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250mg
95%
in stock  
$129.00   $91.00
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500mg
95%
in stock  
$217.00   $152.00
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1g
95%
in stock  
$322.00   $226.00
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5g
95%
in stock  
$966.00   $677.00
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10g
95%
in stock  
$1,449.00   $1,015.00
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA00J2HH
Chemical Name:
1,3,4-Oxadiazol-2-ol
CAS Number:
51517-09-0
Molecular Formula:
C2H2N2O2
Molecular Weight:
86.0495
MDL Number:
MFCD19673344
SMILES:
O=c1ocn[nH]1
Properties
Computed Properties
 
Complexity:
97.7  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
6  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
XLogP3:
-0.2  

Literature

Title: Quantitative structure-activity relationships of 1,3,4-thiadiazol-2(3H)-ones and 1,3,4-oxadiazol-2(3H)-ones as human protoporphyrinogen oxidase inhibitors.

Journal: Bioorganic & medicinal chemistry 20120101

Title: Antimycobacterial activity of new 3,5-disubstituted 1,3,4-oxadiazol-2(3H)-one derivatives. Molecular modeling investigations.

Journal: Bioorganic & medicinal chemistry 20090701

Title: An efficient and expeditious synthesis of di- and trisubstituted amino-phenyl and -benzyl derivatives of tetrazole and [1,3,4]oxadiazol-2-one.

Journal: Journal of combinatorial chemistry 20080101

Title: Keto-1,3,4-oxadiazoles as cathepsin K inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20060601

Title: Elucidation of fatty acid amide hydrolase inhibition by potent alpha-ketoheterocycle derivatives from Monte Carlo simulations.

Journal: Journal of the American Chemical Society 20051214

Title: Antimycobacterial activity of new 3-substituted 5-(pyridin-4-yl)-3H-1,3,4-oxadiazol-2-one and 2-thione derivatives. Preliminary molecular modeling investigations.

Journal: Bioorganic & medicinal chemistry 20050601

Title: Variations of acidic functions at position 2 and substituents at positions 4, 5 and 6 of the indole moiety and their effect on NMDA-glycine site affinity.

Journal: European journal of medicinal chemistry 20031001

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