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  2. 4,4'-Dichlorobenzophenone - Wikipedia

    en.wikipedia.org/wiki/4,4'-dichlorobenzophenone

    4,4’-Dichlorobenzophenone is prepared by the acylation of chlorobenzene with 4-chlorobenzoyl chloride. The conversion is typically conducted in the presence of an aluminium chloride catalyst in a petroleum ether solvent. ClC 6 H 5 C(O)Cl + C 6 H 5 Cl → (ClC 6 H 4) 2 CO + HCl

  3. Bromazolam - Wikipedia

    en.wikipedia.org/wiki/Bromazolam

    This lone pair facilitates a nucleophilic attack, where the nitrogen attacks the carbon of chloroacetyl chloride, inducing a negatively charged oxygen. Subsequently, the oxygen re-establishes the carbon-oxygen double bond, expelling a chloride ion, leading to the formation of bromoacetamide-2-chloro-5-benzophenone.

  4. Bromochlorobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromochlorobenzene

    All three have been synthesized by various routes: 1-Bromo-2-chlorobenzene: from 2-chloroaniline, via diazotization followed by a Sandmeyer reaction [1]; 1-Bromo-3-chlorobenzene: by (3-chlorophenyl)trimethylgermanium by electrophilic substitution [2] [better source needed]

  5. Flubrotizolam - Wikipedia

    en.wikipedia.org/wiki/Flubrotizolam

    Flubrotizolam (2-bromo-4-(2-fluorophenyl)-9-methyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine) is a thienotriazolodiazepine derivative with potent sedative and anxiolytic effects, which has been sold as a designer drug.

  6. Halazone - Wikipedia

    en.wikipedia.org/wiki/Halazone

    Halazone (4-(dichlorosulfamoyl)benzoic acid) is a chemical compound whose formula can be written as either C 7 H 5 Cl 2 NO 4 S or (HOOC)(C 6 H 4)(SO 2)(NCl 2). It has been widely used to disinfect drinking water. Other names for this compound include p-sulfondichloramidobenzoic acid, 4-[(dichloroamino)sulfonyl]benzoic acid, and Pantocide.

  7. Bromobenzyl cyanide - Wikipedia

    en.wikipedia.org/wiki/Bromobenzyl_cyanide

    Bromobenzyl cyanide (BBC), also known in the military idiom as camite (CA), is an obsolete lachrymatory agent [1] introduced in World War I by the Allied Powers, being a standard agent, along with chloroacetophenone, adopted by the CWS. [2]

  8. 2,4,6-Trichlorobenzoyl chloride - Wikipedia

    en.wikipedia.org/.../2,4,6-Trichlorobenzoyl_chloride

    It is the primary reactant in Yamaguchi esterification. 2,4,6-Trichlorobenzoyl chloride readily reacts with alcohols. This newly formed reagent, when mixed with a stoichiometric amount of 4-dimethylaminopyridine, cyclizes and forms esters. This reaction creates 2,4,6-trichlorobenzoic acid as a byproduct.

  9. Management of tuberculosis - Wikipedia

    en.wikipedia.org/wiki/Management_of_tuberculosis

    Management of tuberculosis refers to techniques and procedures utilized for treating tuberculosis (TB), or simply a treatment plan for TB.. The medical standard for active TB is a short course treatment involving a combination of isoniazid, rifampicin (also known as Rifampin), pyrazinamide, and ethambutol for the first two months.

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