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  • ...imides''' are a type of dehydrating chemical most often used to activate [[carboxylic acid]]s for subsequent coupling with primary [[amine]]s, producing an [[amide]] ...ric reaction.png|left|500px|'''Scheme 1''':Coupling of an amide group to a carboxylic acid activated by a carbodiimide.}}
    3 KB (480 words) - 12:22, 27 August 2010
  • ...of ester preparation ([[alcoholysis]]) uses an acid chloride instead of a carboxylic acid. Both methods involve [[nucleophilic acyl substitution]], that is, the repl
    2 KB (299 words) - 07:59, 8 June 2009
  • ...ic group at the other end (as the sodium or ammonium salt), other than a [[carboxylic acid]] salt. Detergents are often synthetic versions of soap, in which the carbo ...oup, sulfate, on the other end. If the sulfate group were replaced with a carboxylic acid salt, this compound would be called a soap. Ammonium ions are also frequen
    2 KB (335 words) - 20:55, 13 March 2012
  • {{r|Carboxylic acid}}
    686 bytes (93 words) - 10:58, 11 January 2010
  • {{r|Carboxylic acid}}
    673 bytes (86 words) - 07:42, 8 January 2010
  • *{{rp|carboxylic acid}}
    215 bytes (24 words) - 08:13, 24 September 2008
  • {{r|Carboxylic acid}}
    171 bytes (19 words) - 10:33, 3 October 2009
  • ...pylcarbodiimide''' is a [[dehydration reagent]] that is used to activate [[carboxylic acid]]s for coupling with either [[alcohol]]s or [[amine]]s to form [[ester]] or
    453 bytes (63 words) - 11:31, 3 October 2009
  • {{r|Carboxylic acid}}
    2 KB (265 words) - 10:53, 11 January 2010
  • ...acin's IUPAC chemical name is 1-ethyl-4-oxo-[1,3]dioxolo[4,5-g]cinnoline-3-carboxylic acid and its chemical formula is C<sub>12</sub>H<sub>10</sub>N<sub>2</sub>O<sub>
    906 bytes (125 words) - 03:06, 16 February 2010
  • ...methylaminopropyl)-carbodiimide is a reagent most often used to activate [[carboxylic acid]]s for subsequent coupling with either [[alcohol]]s or primary [[amine]]s t
    480 bytes (68 words) - 10:12, 13 March 2024
  • ...the food industry. Acids, such as the twenty common [[amino acid]]s and [[carboxylic acid|carboxylic acids]] (including [[valeric acid]], and [[propionic acid]]), ar
    4 KB (691 words) - 08:05, 15 March 2024
  • {{r|Carboxylic acid}}
    319 bytes (34 words) - 10:40, 3 October 2009
  • ...-3-[[4-(pyridin-2-ylsulfamoyl)phenyl]hydrazinylidene]cyclohexa-1,4-diene-1-carboxylic acid and its chemical formula is C<sub>18</sub>H<sub>14</sub>N<sub>4</sub>O<sub
    1 KB (137 words) - 08:55, 8 June 2009
  • ...le bound to an [[oxygen]] atom. Closely related chemical groups include [[carboxylic acid]]s, in which R<sub>1</sub> or R<sub>2</sub> = OH, [[ester]]s, in which R<su
    727 bytes (121 words) - 08:16, 24 September 2008
  • ...at are "a group of derivatives of naphthyridine carboxylic acid, quinoline carboxylic acid, or nalidixic acid."<ref>{{MeSH}}</ref> [[Nadixilic acid]]'s effects are lo
    3 KB (412 words) - 16:33, 2 December 2010
  • ...thyl)-7-[(2-cyanoacetyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, and its chemical formula, C<sub>13</sub>H<sub>13</sub>N<sub>3</sub>O<sub>6
    1 KB (179 words) - 14:39, 13 July 2009
  • ...yimino)acetyl]amino]-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid</nowiki>. It has chemical formula C<sub>14</sub>H<sub>13</sub>N<sub>5</sub>
    823 bytes (118 words) - 15:48, 5 April 2009
  • ...hiadiazol- 2-yl)thio) methyl)-8 -oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid</nowiki>
    878 bytes (120 words) - 13:56, 29 April 2008
  • Foscarnet is a [[carboxylic acid]]-based organic mimic of the natural inorganic compound [[pyrophosphate]].
    3 KB (418 words) - 00:58, 6 February 2010
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