enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Stobbe condensation - Wikipedia

    en.wikipedia.org/wiki/Stobbe_condensation

    The Stobbe condensation entails the reaction of an aldehyde or ketone with an ester of succinic acid to generate alkylidene succinic acid or related derivatives. [1] The reaction consumes one equivalent of metal alkoxide. Commonly, diethylsuccinate is a component of the reaction. The usual product is salt of the half-ester.

  3. Diethyl succinate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_succinate

    It is a colorless liquid with the formula (CH 2 CO 2 Et) 2 (Et = ethyl). The organic molecule contains two ester groups. This ester is a versatile chemical intermediate. A colorless liquid, diethyl succinate is formed by Fischer esterification of succinic acid and ethanol.

  4. Dibasic ester - Wikipedia

    en.wikipedia.org/wiki/Dibasic_ester

    Dibasic ester or DBE is an ester of a dicarboxylic acid.Depending on the application, the alcohol may be methanol or higher molecular weight monoalcohols. Mixtures of different methyl dibasic esters are commercially produced from short-chain acids such as adipic acid, glutaric acid, and succinic acid. [1]

  5. N-Hydroxysuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxysuccinimide

    N-Hydroxysuccinimide (NHS) is an organic compound with the formula (CH 2 CO) 2 NOH. It is a white solid that is used as a reagent for preparing active esters in peptide synthesis. It can be synthesized by heating succinic anhydride with hydroxylamine or hydroxylamine hydrochloride .

  6. 2,2,3,3-Tetramethylsuccinic acid - Wikipedia

    en.wikipedia.org/wiki/2,2,3,3-Tetramethylsuccin...

    In chemistry, 2,2,3,3-tetramethylsuccinic acid or 2,2,3,3-tetramethylbutane-1,4-dioic acid is a dicarboxylic acid with the formula C 8 H 14 O 4, or HOOC-C(CH 3) 2-C(CH 3) 2-COOH. [1] [2] It can be seen as derivative of succinic acid (butane-1,4-dioic acid) with two methyl groups replacing two hydrogen atoms on each of the central carbon atoms ...

  7. Trifluoroacetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_anhydride

    Trifluoroacetic anhydride was originally prepared by the dehydration of trifluoroacetic acid with phosphorus pentoxide. [2] The dehydration might also be carried out with excess α-halogenated acid chlorides. For example, with dichloroacetyl chloride: [3] 2 CF 3 COOH + Cl 2 CHCOCl → (CF 3 CO) 2 O + Cl 2 CHCOOH + HCl

  8. Succinyl chloride - Wikipedia

    en.wikipedia.org/wiki/Succinyl_chloride

    It is the acyl chloride derivative of succinic acid and a simple diacid chloride. It is a colorless liquid. It is a colorless liquid. It used as a reagent in organic synthesis .

  9. Succinic acid - Wikipedia

    en.wikipedia.org/wiki/Succinic_acid

    Succinic acid (/ s ə k ˈ s ɪ n ɪ k /) is a dicarboxylic acid with the chemical formula (CH 2) 2 (CO 2 H) 2. [5] In living organisms, succinic acid takes the form of an anion, succinate, which has multiple biological roles as a metabolic intermediate being converted into fumarate by the enzyme succinate dehydrogenase in complex 2 of the electron transport chain which is involved in making ...