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  2. Osazone - Wikipedia

    en.wikipedia.org/wiki/Osazone

    Osazone formation was developed by Emil Fischer, [3] who used the reaction as a test to identify monosaccharides. The formation of a pair of hydrazone functionalities involves both oxidation and condensation reactions. [4] Since the reaction requires a free carbonyl group, only "reducing sugars" participate.

  3. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    Reagent test Alcohols: Forms Lucas test in alcohols is a test to differentiate between primary, secondary, and tertiary alcohols. Alkaloids: Forms Froehde Liebermann Mandelin Marquis Mayer's Mecke Simon's: Amines, and amino acids: Forms Folin's: Barbiturates: Class Dille–Koppanyi Zwikker: Benzodiazepines: Class Zimmermann: Phytocannabinoids ...

  4. Triethyloxonium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Triethyloxonium_tetrafluo...

    It is often called Meerwein's reagent or Meerwein's salt after its discoverer Hans Meerwein. [2] [3] Also well known and commercially available is the related trimethyloxonium tetrafluoroborate. The compounds are white solids that dissolve in polar organic solvents. They are strong alkylating agents.

  5. Hydrazone - Wikipedia

    en.wikipedia.org/wiki/Hydrazone

    [7] [8] Hydrazone-based coupling methods are used in medical biotechnology to couple drugs to targeted antibodies (see ADC), e.g. antibodies against a certain type of cancer cell. The hydrazone-based bond is stable at neutral pH (in the blood), but is rapidly destroyed in the acidic environment of lysosomes of the cell.

  6. FSA Eligibility List - Wikipedia

    en.wikipedia.org/wiki/FSA_Eligibility_List

    The FSA Eligibility List is a list of tens of thousands of medical items that have been determined to be qualified expenses for flexible spending accounts in the United States. The U.S. Internal Revenue Service outlines eligible product categories in its published guidelines. [ 1 ]

  7. Carbonyl oxidation with hypervalent iodine reagents - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_oxidation_with...

    A key iodine(III) enolate intermediate forms, which then undergoes either nucleophilic substitution (α-functionalization), elimination (dehydrogenation), or rearrangement. Common hypervalent iodine reagents used to effect these transformations include iodosylbenzene (PhIO), [1] Koser's reagent (PhI(OTs)OH), [1] and (dichloroiodo)benzene (PhICl ...

  8. Disodium tetracarbonylferrate - Wikipedia

    en.wikipedia.org/wiki/Disodium_tetracarbonylferrate

    It is always used as a solvate, e.g., with tetrahydrofuran or dimethoxyethane, which bind to the sodium cation. [1] An oxygen-sensitive colourless solid, it is a reagent in organometallic and organic chemical research. The dioxane solvated sodium salt is known as Collman's reagent, in recognition of James P. Collman, an early popularizer of its ...

  9. Ruthenium tetroxide - Wikipedia

    en.wikipedia.org/wiki/Ruthenium_tetroxide

    Ruthenium tetroxide is the inorganic compound with the formula RuO 4.It is a yellow volatile solid that melts near room temperature. [3] It has the odor of ozone. [4] Samples are typically black due to impurities.

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