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Amino radical: Difference between revisions

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Revision as of 20:17, 7 September 2011 editKatharineamy (talk | contribs)Extended confirmed users, Pending changes reviewers, Rollbackers144,640 edits added Category:Inorganic compounds; removed {{uncategorized}} using HotCat← Previous edit Revision as of 06:31, 9 September 2011 edit undoCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'KEGG_Ref') per Chem/Drugbox validation (report errors or [[user talk:CheMoBoNext edit →
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{{Chembox {{Chembox
| verifiedrevid = 448993879
| SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:29318)|work = Chemical Entities of Biological Interest (ChEBI)|location = UK|publisher = European Bioinformatics Institute|at = IUPAC Names}}</ref> (substitutive)<br /> | SystematicName = Azanyl<ref name = "aminyl (CHEBI:29318)">{{Cite web|url = https://www.ebi.ac.uk/chebi/searchId.do?chebiId=29318|title = aminyl (CHEBI:29318)|work = Chemical Entities of Biological Interest (ChEBI)|location = UK|publisher = European Bioinformatics Institute|at = IUPAC Names}}</ref> (substitutive)<br />
Dihydridonitrogen(•)<ref name = "aminyl (CHEBI:29318)" /> (additive) Dihydridonitrogen(•)<ref name = "aminyl (CHEBI:29318)" /> (additive)

Revision as of 06:31, 9 September 2011

Amino radical
Names
Systematic IUPAC name Azanyl (substitutive)
Dihydridonitrogen(•) (additive)
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/H2N/h1H2Key: MDFFNEOEWAXZRQ-UHFFFAOYSA-N
SMILES
Properties
Chemical formula NH
2
Molar mass 16.0226 g mol
Thermochemistry
Std molar
entropy
(S298)
194.71 J K mol
Std enthalpy of
formation
fH298)
190.37 kJ mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

The azanyl radical, NH
2
, is the neutral form of the amide ion (NH
2). Azanyl radicals are highly reactive and consequently short lived; however, they form an important part of radical chemistry. In sufficiently high concentration, azanyl dimerises to form hydrazine.

References

  1. ^ "aminyl (CHEBI:29318)". Chemical Entities of Biological Interest (ChEBI). UK: European Bioinformatics Institute. IUPAC Names.




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