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  1. The air oxidation of toluene is the source of the majority of the world's synthetic benzaldehyde. Both vapor- and liquid-phase air oxidation processes have been used. In the vapor-phase process, a mixture of air and toluene vapor is passed over a catalyst consisting of the oxides of uranium, molybdenum, or related metals.

    • Pyrrolidine

      Computed by PubChem 2.2 (PubChem release 2021.10.14) Dates....

  2. en.wikipedia.org › wiki › BenzaldehydeBenzaldehyde - Wikipedia

    Benzaldehyde (C 6 H 5 CHO) is an organic compound consisting of a benzene ring with a formyl substituent. It is among the simplest aromatic aldehydes and one of the most industrially useful. It is a colorless liquid with a characteristic almond -like odor, and is commonly used in cherry -flavored sodas. [5]

    • C₇H₆O
    • 106.124 g·mol−1
    • −57.12 °C (−70.82 °F; 216.03 K)
    • 6.95 g/L (25 °C)
  3. Benzaldehyde. Molecular Formula CHO. Average mass 106.122 Da. Monoisotopic mass 106.041862 Da. ChemSpider ID 235.

  4. Quantity Value Units Method Reference Comment; T boil: 452. ± 7. K: AVG: N/A: Average of 13 values; Individual data points Quantity Value Units Method Reference Comment; T fus: 247. K: N/A: Buckingham and Donaghy, 1982

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  6. IUPAC Standard InChIKey: HUMNYLRZRPPJDN-UHFFFAOYSA-N Copy CAS Registry Number: 100-52-7 Chemical structure: This structure is also available as a 2d Mol file or as a computed 3d SD file

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