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  2. Molisch's test - Wikipedia

    en.wikipedia.org/wiki/Molisch's_test

    Molisch test (using α-napthol) indicating a positive result (see purple ring). Molisch's test is a sensitive chemical test, named after Austrian botanist Hans Molisch, for the presence of carbohydrates, based on the dehydration of the carbohydrate by sulfuric acid or hydrochloric acid to produce an aldehyde, which condenses with two molecules of a phenol (usually α-naphthol, though other ...

  3. N,N'-Diisopropylcarbodiimide - Wikipedia

    en.wikipedia.org/wiki/N,N'-Diisopropylcarbodiimide

    External MSDS: Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ...

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. Hans Molisch - Wikipedia

    en.wikipedia.org/wiki/Hans_Molisch

    Hans Molisch (6 December 1856, Brünn, Habsburg Moravia - 8 December 1937, Wien, Austria) was a Czech-Austrian botanist. Molisch's test is named after him, it is a sensitive chemical test for the presence of carbohydrates .

  6. tert-Butyldimethylsilyl chloride - Wikipedia

    en.wikipedia.org/wiki/Tert-Butyldimethylsilyl...

    tert-Butyldimethylsilyl chloride is an organosilicon compound with the formula (Me 3 C)Me 2 SiCl (Me = CH 3).It is commonly abbreviated as TBSCl or TBDMSCl. It is a chlorosilane containing two methyl groups and a tert-butyl group.

  7. 1,8-Diazabicyclo (5.4.0)undec-7-ene - Wikipedia

    en.wikipedia.org/wiki/1,8-Diazabicyclo(5.4.0...

    As a reagent in organic chemistry, DBU is used as a ligand and base. As a base, protonation occurs at the imine nitrogen. [5] Lewis acids also attach to the same nitrogen. [6] These properties recommend DBU for use as a catalyst, for example as a curing agent for epoxy resins and polyurethane.

  8. Pyridinium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Pyridinium_p-toluenesulfonate

    In organic synthesis, PPTS is used as a weakly acidic catalyst, providing an organic soluble source of pyridinium (C 5 H 5 NH +) ions.For example, PPTS is used to deprotect silyl ethers or tetrahydropyranyl ethers when a substrate is unstable to stronger acid catalysts.

  9. Furfural - Wikipedia

    en.wikipedia.org/wiki/Furfural

    Determining the structure of furfural required some time: the furfural molecule contains a cyclic ether , which tends to break open when it's treated with harsh reagents. In 1870, German chemist Adolf von Baeyer speculated about the structure of the chemically similar compounds furan and 2-furoic acid . [ 11 ]