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  • ...te, which is the conjugate base of [[benzoic acid]]. [[Acetic acid]] is a carboxylic acid that gives vinegar its bite. [[Formic acid]] has historically been used to ...Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to f
    2 KB (398 words) - 15:31, 8 March 2023
  • 12 bytes (1 word) - 16:43, 4 December 2007
  • 101 bytes (15 words) - 18:06, 17 July 2008
  • Auto-populated based on [[Special:WhatLinksHere/Carboxylic acid]]. Needs checking by a human.
    681 bytes (92 words) - 11:40, 11 January 2010
  • 29 bytes (3 words) - 12:47, 4 July 2009

Page text matches

  • ...d''', HCOOH, also known as methanoic acid, is the simplest member of the [[carboxylic acid]]s, RCOOH (where R = H, or any alkyl group). It is a pungent liquid which i Formic acid is a stronger acid than any other member of the unsubstituted carboxylic acid series, and forms salts, called formates, which (except for those of lead a
    613 bytes (100 words) - 15:10, 12 April 2008
  • An omega-3 fatty acid consisting of a carboxylic acid with a 22-carbon chain, and six cis double bonds.
    140 bytes (21 words) - 10:07, 3 September 2009
  • <noinclude>{{Subpages}}</noinclude>Carboxylic acid form of vitamin A, also known as all-trans retinoic acid or ATRA, is a topi
    198 bytes (30 words) - 09:28, 28 November 2013
  • * trans-4-aminomethylcyclohexane-1-carboxylic acid
    563 bytes (50 words) - 17:33, 22 October 2010
  • A [[dehydration reagent]] used to couple [[carboxylic acid]]s with [[alohol]]s or [[amine]]s.
    129 bytes (18 words) - 11:05, 3 October 2009
  • Chemical used to synthesize activated, semi-stable [[carboxylic acid]] [[esters]] for subsequent coupling reactions.
    152 bytes (16 words) - 09:29, 7 October 2009
  • ...te, which is the conjugate base of [[benzoic acid]]. [[Acetic acid]] is a carboxylic acid that gives vinegar its bite. [[Formic acid]] has historically been used to ...Conversely, the [[Fisher esterification]] reaction can be used to react a carboxylic acid with an alcohol to form an ester. Carboxylic acids can also be reduced to f
    2 KB (398 words) - 15:31, 8 March 2023
  • ...s closely related to the acidic amino acid [[glutamic acid]] which has a [[carboxylic acid]] in place of the amide group present in glutamine. Glutamine is a neutral
    547 bytes (87 words) - 08:08, 8 June 2009
  • A [[carbodiimide]] used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.
    138 bytes (19 words) - 11:33, 3 October 2009
  • Dehydrating chemical mostly used to couple [[carboxylic acid]]s with primary [[amine]]s, producing an [[amide]] compound.
    157 bytes (20 words) - 10:36, 3 October 2009
  • A [[carbodiimide]] reagent mostly used to activate [[carboxylic acid]]s for coupling with [[alcohol]]s or [[amine]]s.
    153 bytes (21 words) - 10:31, 3 October 2009
  • ...NHS) is chemical used to form semi-stable, but reactive, [[ester]]s from [[carboxylic acid]]s. Such NHS esters can be stored for a relatively long time if kept cold a ...diimide coupling via NHS ester.png|left|350px|'''Scheme 1''':Coupling of a carboxylic acid and a primary amine via O-acylisourea ester and NHS ester intermediates.}}
    1 KB (235 words) - 10:55, 9 January 2010
  • Auto-populated based on [[Special:WhatLinksHere/Carboxylic acid]]. Needs checking by a human.
    681 bytes (92 words) - 11:40, 11 January 2010
  • HCO<sub>2</sub>H, the smallest [[carboxylic acid]], and the sting delivered by stinging [[nettle]]s and [[ant]]s.
    149 bytes (22 words) - 11:14, 13 July 2008
  • ...c acid''', formula CH<sub>3</sub>CO<sub>2</sub>H, is the second smallest [[carboxylic acid]] and is larger than only [[formic acid]], HCO<sub>2</sub>H. Vinegar's tar
    832 bytes (128 words) - 08:12, 15 March 2024
  • {{r|Carboxylic acid}}
    545 bytes (73 words) - 16:37, 11 January 2010
  • {{r|carboxylic acid}}
    178 bytes (23 words) - 16:09, 4 November 2010
  • '''N,N'-dicyclohexylcarbodiimide''' is carbodiimide reagent used to couple [[carboxylic acid]]s with either [[alcohol]]s or [[amine]]s to form [[ester]]s or [[amide]]s.
    288 bytes (35 words) - 11:03, 3 October 2009
  • ...rred to as an [[amino acid]] despite the fact that it does not contain a [[carboxylic acid]] group like most amino acids do. It plays an important role in the phase
    3 KB (353 words) - 11:31, 11 December 2010
  • ...into the carbonyl system. This makes the carbonyl less reactive than most carboxylic acid derivatives in [[electrophile|electrophilic]] substitution reactions, and m *Reaction of most other [[carboxylic acid]] derivatives with ammonia, a primary amine, or a secondary amine will give
    3 KB (410 words) - 02:51, 17 October 2013
  • ...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
  • ...ethylideneamino)-6-[(1R,2R)-1,2,3-trihydroxypropyl]-5,6-dihydro-4H-pyran-2-carboxylic acid and its chemical formula is C<sub>12</sub>H<sub>20</sub>N<sub>4</sub>O<sub>
    1 KB (178 words) - 12:31, 21 January 2009
  • ...ving it a molecular mass of 159.23 g/mol. It is both an [[amine]] and a [[carboxylic acid]].
    2 KB (306 words) - 14:40, 13 February 2011
  • |iupac=4-(aminomethyl)cyclohexane-1-carboxylic acid
    4 KB (458 words) - 17:34, 22 October 2010
  • ...-2-amino-2-phenylacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, and its molecule formula, C<sub>18</sub>H<sub>19</sub>N<sub>3</sub>O<sub>6
    1 KB (147 words) - 15:52, 13 July 2009
  • ...with the four carbon carboxylic acid, oxaloacetate--to form the six carbon carboxylic acid, citrate.
    8 KB (1,089 words) - 02:01, 2 June 2009
  • ...-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid.
    1 KB (151 words) - 11:38, 13 July 2009
  • ...methoxycarbonylamino]-2-ethyl-6-trifluoromethyl-3,4-dihydro-2H-quinoline-1-carboxylic acid ethyl ester. The drug has a formula weight of 600.47 g/mol and is registere
    1 KB (181 words) - 14:03, 26 November 2010
  • ...chemical name is 1-cyclopropyl-6-fluoro-4-oxo-7-piperazin-1-ylquinoline-3-carboxylic acid and it has chemical formula C<sub>17</sub>H<sub>18</sub>FN<sub>3</sub>O<sub
    1 KB (185 words) - 06:34, 8 June 2009
  • ...tyl]amino]-8-oxo-3-[(E)-prop-1-enyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. It has a molecule formula C<sub>18</sub>H<sub>19</sub>N<sub>3</sub>O<sub>
    1 KB (178 words) - 13:42, 13 July 2009
  • ...-carbonyl)amino]-2-phenylacetyl]amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid and it has chemical formula C<sub>20</sub>H<sub>23</sub>N<sub>5</sub>O<sub>
    1 KB (178 words) - 06:19, 8 June 2009
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