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2. Cyclohexanone - Wikipedia

   en.wikipedia.org/wiki/Cyclohexanone

   Cyclohexanone is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [11]. C 6 H 12 + O 2 → (CH 2) 5 CO + H 2 O. This process forms cyclohexanol as a by-product, and this mixture, called "KA Oil" for ketone-alcohol oil, is the main feedstock for the production of adipic acid.

3. List of compounds with carbon number 6 - Wikipedia

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

   cyclohexanone: 108-94-1 C 6 H 10 O: cyclohexene oxide: 286-20-4 C 6 H 10 O: hexenal: 1335-39-3 C 6 H 10 O: meparfynol: 77-75-8 C 6 H 10 OS: allyl thiopropionate: 41820-22-8 C 6 H 10 OS 2: allicin: 539-86-6 C 6 H 10 O 2: cyclobutanecarboxylic acid methyl ester: 765-85-5 C 6 H 10 O 2: cyclobutyl ethanoate: 500033-42-1 C 6 H 10 O 2: cyclopentane ...

4. Cyclohexane (data page) - Wikipedia

   en.wikipedia.org/wiki/Cyclohexane_(data_page)

   The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions.

5. Immediately dangerous to life or health - Wikipedia

   en.wikipedia.org/wiki/Immediately_dangerous_to...

   108-93-0: 0243: Cyclohexanol: 1640 mg/m 3: 400 ppm: 108930: 108-94-1: 0425: Cyclohexanone: 2814 mg/m 3: 700 ppm: 108941: 110-83-8: 1054: Cyclohexene: 6720 mg/m 3: 2000 ppm: 110838: 542-92-7: 0857: Cyclopentadiene: 2025 mg/m 3: 750 ppm: 542927 (10% Lower explosive limit LEL) 13121-70-5-Cyhexatin: 80 mg/m 3 (25 mg/m 3 - for Sn)-tin-org: 94-75-7: ...

6. Cyclohexanol - Wikipedia

   en.wikipedia.org/wiki/Cyclohexanol

   Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.

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   Money market funds earn higher base returns, starting above 1%, with some funds paying up to 4.00% or more. With a fund, you risk losing money if the market takes a severe downturn.

9. Cycloheptanone - Wikipedia

   en.wikipedia.org/wiki/Cycloheptanone

   The resulting sodium salt of 1-(nitromethyl)cyclohexanol is added to acetic acid and shaken with hydrogen gas in the presence of W-4 Raney nickel catalyst. Sodium nitrite and acetic acid are then added to give cycloheptanone. [5] Cycloheptanone is also prepared by ring expansion of cyclohexanone with diazomethane as the methylene source. [5]