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  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. 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.

  4. Diaminomaleonitrile - Wikipedia

    en.wikipedia.org/wiki/Diaminomaleonitrile

    Photochemical rearrangement of DAMN under UV light gives 4-aminoimidazole-5-carbonitrile (AICN), which can react further to form various nucleobases. [8] [9] Early experiments have also suggested that certain amino acids, such as aspartic acid, alanine, and glycine, may have their probiotic origins in the acidic hydrolysis of diaminomaleonitrile.

  5. Ethyl cyanoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_cyanoacetate

    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; Ethyl cyanoacetate is a building block for the synthesis of heterocycles which are used for ...

  6. 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.

  7. 2-Hydroxy-5-methoxybenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Hydroxy-5...

    It reacts with malononitrile to form 2-imino-6-methoxy-2H-1-benzopyran-3-carbonitrile. [2] It can be reduced by sodium borohydride in ethanol to form 2-hydroxy-5-methoxybenzyl alcohol. [ 3 ]

  8. CS gas - Wikipedia

    en.wikipedia.org/wiki/CS_gas

    The compound 2-chlorobenzalmalononitrile (also called o-chlorobenzylidene malononitrile; chemical formula: C 10 H 5 ClN 2), a cyanocarbon, is the defining component of the lachrymatory agent commonly referred to as CS gas, a tear gas which is used as a riot control agent, and is banned for use in warfare due to the 1925 Geneva Protocol.

  9. Tetramethylsuccinonitrile - Wikipedia

    en.wikipedia.org/wiki/Tetramethylsuccinonitrile

    Tetramethylsuccinonitrile or TMSN is an organic compound with the formula (C(CH 3) 2 CN) 2, classified as a dinitrile, and a colorless and odorless solid derived from 2,2'-azobis-isobutyronitrile, a common radical initiator in the manufacture of PVC: [(CH 3) 2 C(CN)] 2 N 2 → [(CH 3) 2 C(CN)] 2 + N 2. [6]