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  2. Isoxazole - Wikipedia

    en.wikipedia.org/wiki/Isoxazole

    Meanwhile, the azirine intermediate can react with nucleophiles, especially carboxylic acids. Given the photoreactions, isoxazole group is developed as a native photo-cross-linker for photoaffinity labeling and chemoproteomic studies.

  3. Carbamic acid - Wikipedia

    en.wikipedia.org/wiki/Carbamic_acid

    Carbamic acid is a planar molecule. [3]The H 2 N− group of carbamic acid, unlike that of most amines, cannot be protonated to an ammonium group H 3 N + −.The zwitterionic form H 3 N + −COO − is very unstable and promptly decomposes into ammonia and carbon dioxide, [6] yet there is a report of its detection in ices irradiated with high-energy protons.

  4. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    Formic acid (HCO 2 H) 3.75 Chloroformic acid (ClCO 2 H) 0.27 [5] Acetic acid (CH 3 CO 2 H) 4.76 Glycine (NH 2 CH 2 CO 2 H) 2.34 Fluoroacetic acid (FCH 2 CO 2 H) 2.586 Difluoroacetic acid (F 2 CHCO 2 H) 1.33 Trifluoroacetic acid (CF 3 CO 2 H) 0.23 Chloroacetic acid (ClCH 2 CO 2 H) 2.86 Dichloroacetic acid (Cl 2 CHCO 2 H) 1.29 Trichloroacetic ...

  5. Dimethylcarbamoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Dimethylcarbamoyl_chloride

    To suppress the formation of ureas, excess phosgene is used (in a 3:1 ratio). The reaction can also be carried out at the laboratory scale with diphosgene or triphosgene and an aqueous dimethylamine solution in the two-phase system of benzene–xylene and water in a stirred reactor with sodium hydroxide as an acid scavenger. However ...

  6. Phenylboronic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylboronic_acid

    Phenylboronic acid or benzeneboronic acid, abbreviated as PhB(OH) 2 where Ph is the phenyl group C 6 H 5 - and B(OH) 2 is a boronic acid containing a phenyl substituent and two hydroxyl groups attached to boron. Phenylboronic acid is a white powder and is commonly used in organic synthesis.

  7. Carbamoyl chloride - Wikipedia

    en.wikipedia.org/wiki/Carbamoyl_chloride

    In a reaction that is typically avoided, hydrolysis of carbamoyl chlorides gives carbamic acids: R 2 NCOCl + H 2 O → R 2 NC(O)OH + HCl. Owing to the influence of the amino group, these compounds are less hydrolytically sensitive than the usual acid chlorides. A related but more useful reaction is the analogous reaction with alcohols: [2]

  8. Prisoners of Profit - The Huffington Post

    projects.huffingtonpost.com/projects/prisoners...

    In a complex arrangement, Slattery gave up a portfolio of 14 immigration detention facilities and adult prisons across the country as part of a $62 million sale, while buying back one division for $3.75 million: Youth Services International. As this new Slattery venture continued to grow in Florida, the old problems surfaced again.

  9. Carbamate - Wikipedia

    en.wikipedia.org/wiki/Carbamate

    H 2 NCO − 2 + 2 H 2 O ⇌ NH + 4 + HCO − 3 + OH − H 2 NCO − 2 + H 2 O ⇌ NH + 4 + CO 2− 3. Calcium carbamate is soluble in water, whereas calcium carbonate is not. Adding a calcium salt to an ammonium carbamate/carbonate solution will precipitate some calcium carbonate immediately, and then slowly precipitate more as the carbamate ...