enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Malononitrile

    Malononitrile is an organic compound nitrile with the formula CH 2 (CN) 2. It is a colorless or white solid, although aged samples appear yellow or even brown. It is a colorless or white solid, although aged samples appear yellow or even brown.

  3. Diaminomaleonitrile - Wikipedia

    en.wikipedia.org/wiki/Diaminomaleonitrile

    The cis-configuration of the amino groups was shown in 1928 through reaction with glyoxal to give 2,3-diaminopyrazine, and the full structure was shown in 1955 to be diaminomaleonitrile, as opposed to the isomeric aminoiminosuccinonitrile (AISN). [5] It can be prepared by cyanation of aminomalonitrile. [6] [7]

  4. Solvent Yellow 7 - Wikipedia

    en.wikipedia.org/wiki/Solvent_Yellow_7

    Like most azobenzenes, Solvent Yellow 7 can be synthesized by the reaction of the phenyldiazonium salt with phenol.The optimal pH value for this azo coupling is 8.5-10. The reaction is carried out in water, since sodium chloride (or potassium chloride) formed in the reaction is soluble in water, while the product precipitates.

  5. Carbonyl cyanide m-chlorophenyl hydrazone - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_cyanide_m-chloro...

    Carbonyl cyanide m-chlorophenyl hydrazone (CCCP; also known as [(3-chlorophenyl)hydrazono]malononitrile) is a chemical inhibitor of oxidative phosphorylation. It is a nitrile , hydrazone and protonophore .

  6. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    As a safe cyanide-donor reagent [10] Nucleophilic attack at the ester group, as part of acyl substitution: reaction with ammonia leads to cyanoacetamide, which can be converted by dehydration with PCl 5 or POCl 3 to malononitrile. [11] Via the acidic methylene group as a nucleophile

  7. Tetracyanoethylene - Wikipedia

    en.wikipedia.org/wiki/Tetracyanoethylene

    TCNE is prepared by brominating malononitrile in the presence of potassium bromide to give the KBr-complex, and dehalogenating with copper. [1] Oxidation of TCNE with hydrogen peroxide gives the corresponding epoxide, which has unusual properties. [2] In the presence of base, TCNE reacts with malononitrile to give salts of pentacyanopropenide: [3]

  8. Oil Red O - Wikipedia

    en.wikipedia.org/wiki/Oil_Red_O

    Oil Red O (Solvent Red 27, Sudan Red 5B, C.I. 26125, C 26 H 24 N 4 O) is a lysochrome (fat-soluble dye) diazo dye used for staining of neutral triglycerides and lipids on frozen sections and some lipoproteins on paraffin sections.

  9. Sodium maleonitriledithiolate - Wikipedia

    en.wikipedia.org/wiki/Sodium_maleonitriledithiolate

    Sodium maleonitriledithiolate is the chemical compound described by the formula Na 2 S 2 C 2 (CN) 2. The name refers to the cis compound, structurally related to maleonitrile ((CH(CN)) 2). Maleonitriledithiolate is often abbreviated mnt. It is a "dithiolene", i.e. a chelating alkene-1,2-dithiolate.