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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. C-1027 - Wikipedia

    en.wikipedia.org/wiki/C-1027

    The structure of C-1027 is composed of a nine-membered enediyne complex, a deoxygenated aminosugar, a β-amino acid, and a benzoxazolinate moiety. Enediynes contain a double bond between two triple bonds, and their biosynthesis is distinct from other known polyketide and fatty-acid synthesis paradigms.

  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. Infrared spectroscopy correlation table - Wikipedia

    en.wikipedia.org/wiki/Infrared_spectroscopy...

    Bond Type of bond Specific type of bond Absorption peak (cm −1) Appearance C─H alkyl methyl 1260 strong 1380 weak 2870 medium to strong 2960 medium to strong methylene: 1470 strong 2850 medium to strong 2925 medium to strong methine: 2890 weak vinyl: C═CH 2: 900 strong 2975 medium 3080 medium C═CH 3020 medium monosubstituted alkenes ...

  6. 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 ...

  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. CHNOPS - Wikipedia

    en.wikipedia.org/wiki/CHNOPS

    Graphic representation of carbon, hydrogen, nitrogen, oxygen, phosphorus, and sulfur. CHNOPS and CHON are mnemonic acronyms for the most common elements in living organisms. . "CHON" stands for carbon, hydrogen, oxygen, and nitrogen, which together make up more than 95 percent of the mass of biological system