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  2. Trifluoromethanesulfonic anhydride - Wikipedia

    en.wikipedia.org/wiki/Trifluoromethanesulfonic...

    Trifluoromethanesulfonic anhydride, also known as triflic anhydride, is the chemical compound with the formula (CF 3 SO 2) 2 O. It is the acid anhydride derived from triflic acid.

  3. List of compounds with carbon number 2 - Wikipedia

    en.wikipedia.org/wiki/List_of_compounds_with...

    C 2 F 6 O 5 S 2: trifluoromethanesulfonic anhydride: 358-23-6 C 2 F 7 N: perfluoroethanamine: 354-80-3 C 2 H: ethynyl radical: 2122-48-7 C 2 HBrClF 3: halothane: 151-67-7 C 2 HBrO: bromoketene: 78957-22-9 C 2 HBr 2 FO 2: dibromofluoroacetic acid: 353-99-1 C 2 HBr 3: tribromoethene: 598-16-3 C 2 HBr 3 O 2: tribromoacetic acid: 75-96-7 C 2 HClO ...

  4. List of CAS numbers by chemical compound - Wikipedia

    en.wikipedia.org/wiki/List_of_CAS_numbers_by...

    13775–53–6 Na 3 Co(NO 2) 6: sodium cobaltnitrite: 14649–73–1 Na 3 PO 4: sodium phosphate: 7601–54–9 Na 3 Sb: sodium antimonide: 12058–86–5 Na 3 SbS 4: sodium thioantimonide: 13776–84–6 Na 3 VO 4: sodium vanadate: 13721–39–6 Na 4 C 4 H 4 O 6: sodium tartrate: 868–18–8 Na 4 FeC 6 N 6: sodium ferrocyanide: 13601–19 ...

  5. Isopentenyl pyrophosphate - Wikipedia

    en.wikipedia.org/wiki/Isopentenyl_pyrophosphate

    Isopentenyl pyrophosphate (IPP, isopentenyl diphosphate, or IDP) [1] is an isoprenoid precursor. IPP is an intermediate in the classical, HMG-CoA reductase pathway (commonly called the mevalonate pathway) and in the non-mevalonate MEP pathway of isoprenoid precursor biosynthesis.

  6. Dioleoyl-3-trimethylammonium propane - Wikipedia

    en.wikipedia.org/wiki/Dioleoyl-3-trimethyl...

    1,2-Dioleoyl-3-trimethylammonium propane (often abbreviated DOTAP or 18:1TAP) is a di-chain, or gemini, cationic surfactant.It is most commonly encountered as an active ingredient in certain fabric softeners.

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  8. Dimethylcarbamoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Dimethylcarbamoyl_chloride

    [6] Synthesis of dimethylcarbamoyl chloride from chloramine. DMCC can also be formed in small amounts (up to 20 ppm) from dimethylformamide (DMF) in the Vilsmeier–Haack reaction [7] or when DMF is used as a catalyst in the reaction of carboxylic acids with thionyl chloride to the corresponding acyl chloride. [8]

  9. Furfural - Wikipedia

    en.wikipedia.org/wiki/Furfural

    George Fownes named this oil "furfurol" in 1845 (from furfur (bran), and oleum (oil)). [9] In 1848, the French chemist Auguste Cahours determined that furfural was an aldehyde . [ 10 ] Determining the structure of furfural required some time: the furfural molecule contains a cyclic ether ( furan ), which tends to break open when it's treated ...