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  2. Crotonaldehyde - Wikipedia

    en.wikipedia.org/wiki/Crotonaldehyde

    The E-isomer is more common (data given in Table is for the E-isomer). This lachrymatory liquid is moderately soluble in water and miscible in organic solvents. As an unsaturated aldehyde, crotonaldehyde is a versatile intermediate in organic synthesis. It occurs in a variety of foodstuffs, e.g. soybean oils. [4]

  3. File:EUR 2017-212.pdf - Wikipedia

    en.wikipedia.org/wiki/File:EUR_2017-212.pdf

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  4. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    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 ]

  5. C–H···O interaction - Wikipedia

    en.wikipedia.org/wiki/C–H···O_interaction

    Bond strength is less than 1 kcal/mol. In the case of aromatic C–H donors, C–H···O interactions are not linear due to influence of aromatic ring substituents near the interacting C-H group. [ 6 ] [ 7 ] If aromatic molecules involved in С–Н···О interaction belong to the group of polycyclic aromatic hydrocarbons , the strength of C ...

  6. 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.

  7. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde forms cross-links by first combining with a protein to form methylol, which loses a water molecule to form a Schiff base. [47] The Schiff base can then react with DNA or protein to create a cross-linked product. [47] This reaction is the basis for the most common process of chemical fixation.

  8. Bond order - Wikipedia

    en.wikipedia.org/wiki/Bond_order

    In chemistry, bond order is a formal measure of the multiplicity of a covalent bond between two atoms. As introduced by Gerhard Herzberg, [1] building off of work by R. S. Mulliken and Friedrich Hund, bond order is defined as the difference between the numbers of electron pairs in bonding and antibonding molecular orbitals.

  9. Inorganic compound - Wikipedia

    en.wikipedia.org/wiki/Inorganic_compound

    An inorganic compound is typically a chemical compound that lacks carbon–hydrogen bonds⁠ ‍ — ‍ that is, a compound that is not an organic compound. [1] [2] The study of inorganic compounds is a subfield of chemistry known as inorganic chemistry.