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  2. 2,4-Dichlorophenoxyacetic acid - Wikipedia

    en.wikipedia.org/wiki/2,4-Dichlorophenoxyacetic_acid

    2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.

  3. 2,4-DB - Wikipedia

    en.wikipedia.org/wiki/2,4-DB

    2,4-DB or 4-(2,4-dichlorophenoxy)butyric acid is a selective systemic phenoxy herbicide used to control many annual and perennial broad-leaf weeds in alfalfa, peanuts, soybeans, and other crops. Its active metabolite , 2,4-D , inhibits growth at the tips of stems and roots.

  4. Herbicide - Wikipedia

    en.wikipedia.org/wiki/Herbicide

    While the full work of the unit remained secret, certain discoveries were developed for commercial use after the war, including the 2,4-D compound. [15] When 2,4-D was commercially released in 1946, it became the first successful selective herbicide, triggering a worldwide revolution in agricultural output.

  5. Agent Purple - Wikipedia

    en.wikipedia.org/wiki/Agent_Purple

    Agent Purple was chemically similar to the better-known Agent Orange, both of them were consisting of a mixture of the herbicides 2,4-D and 2,4,5-T and in both cases the 2,4-D and 2,4,5-T constituted equal shares of the Agent. [1] The difference was in the form of 2,4,5-T.

  6. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    The addition of hydrogen and an amino group (NR 2) using reagents other than the amine HNR 2 is known as a "formal hydroamination" reaction. Although the advantages of atom economy and/or ready available of the nitrogen source are diminished as a result, the greater thermodynamic driving force, as well as ability to tune the aminating reagent ...

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  8. UNC alum files for 2-word trademark after Bill Belichick ...

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  9. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of an acidic proton next to a carbonyl (C=O) functional group by formaldehyde (H−CHO) and a primary or secondary amine (−NH 2) or ammonia (NH 3). [1] The final product is a β-amino-carbonyl compound also known as a Mannich base.

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