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  2. 4,7-Dichloroquinoline - Wikipedia

    en.wikipedia.org/wiki/4,7-Dichloroquinoline

    4,7-Dichloroquinoline was first reported in a patent filed by IG Farben in 1937. [2] However, its synthesis was not investigated in detail until chloroquine was developed as an antimalarial drug. [ 3 ] : 130–132 A route to the intermediate starting from 3-chloroaniline was developed by chemists at Winthrop Chemical Co .

  3. International Chemical Identifier - Wikipedia

    en.wikipedia.org/wiki/International_Chemical...

    The International Chemical Identifier (InChI, pronounced / ˈ ɪ n tʃ iː / IN-chee) [3] is a textual identifier for chemical substances, designed to provide a standard way to encode molecular information and to facilitate the search for such information in databases and on the web.

  4. CAS Registry Number - Wikipedia

    en.wikipedia.org/wiki/CAS_Registry_Number

    Screenshot of the CAS Common Chemistry database with information about caffeine ().. A CAS Registry Number [1] (also referred to as CAS RN [2] or informally CAS Number) is a unique identification number, assigned by the Chemical Abstracts Service (CAS) in the US to every chemical substance described in the open scientific literature, in order to index the substance in the CAS Registry.

  5. Chloroquine - Wikipedia

    en.wikipedia.org/wiki/Chloroquine

    Chloroquine (CQ) then becomes protonated (to CQ 2+), as the digestive vacuole is known to be acidic (pH 4.7); chloroquine then cannot leave by diffusion. Chloroquine caps hemozoin molecules to prevent further biocrystallization of heme, thus leading to heme buildup.

  6. Template : Did you know nominations/4,7-Dichloroquinoline

    en.wikipedia.org/.../4,7-Dichloroquinoline

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  7. Gould–Jacobs reaction - Wikipedia

    en.wikipedia.org/wiki/Gould–Jacobs_reaction

    A 6 electron cyclization reaction with the loss of another ethanol molecule forms a quinoline (ethyl 4-oxo-4,4a-dihydroquinoline-3-carboxylate). The enol form can be represented from the keto form through keto-enol tautomerism. Protonation of the nitrogen forms ethyl 4-oxo-1,4-dihydroquinoline-3-carboxylate. Mechanism for the Gould-Jacobs reaction

  8. Add, remove, Cc, and Bcc recipients to an email in AOL ...

    help.aol.com/articles/add-remove-cc-and-bcc...

    No one sees who's in the Bcc list beside you. 1. Launch Desktop Gold. 2. Sign on with your username and password. 3. Click the Write icon at the top of the window. 4. Click in the Cc field (or click the Bcc button) and start typing an email address and select it from the drop-down or click the Address Book icon . 5.

  9. Category:Quinolines - Wikipedia

    en.wikipedia.org/wiki/Category:Quinolines

    This category has the following 7 subcategories, out of 7 total. D. Dibenzoquinolines (8 P) P. Pyridazinoquinolines (1 P) Q. ... 4,7-Dichloroquinoline ...