CHEBI:28024 - cyanic acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name cyanic acid
ChEBI ID CHEBI:28024
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:3968, CHEBI:23422
Supplier Information No supplier information found for this compound.
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Formula CHNO
Net Charge 0
Average Mass 43.025
Monoisotopic Mass 43.00581
InChI InChI=1S/CHNO/c2-1-3/h3H
InChIKey XLJMAIOERFSOGZ-UHFFFAOYSA-N
SMILES OC#N
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cyanic acid (CHEBI:28024) is a one-carbon compound (CHEBI:64708)
cyanic acid (CHEBI:28024) is a pseudohalogen oxoacid (CHEBI:23423)
cyanic acid (CHEBI:28024) is conjugate acid of cyanate (CHEBI:29195)
cyanic acid (CHEBI:28024) is tautomer of isocyanic acid (CHEBI:29202)
Incoming cyanates (CHEBI:23420) has functional parent cyanic acid (CHEBI:28024)
cyanate (CHEBI:29195) is conjugate base of cyanic acid (CHEBI:28024)
isocyanic acid (CHEBI:29202) is tautomer of cyanic acid (CHEBI:28024)
IUPAC Names
hydrogen nitridooxocarbonate
hydroxidonitridocarbon
nitridooxocarbonic acid
Synonyms Sources
[C(N)OH] IUPAC
acide cyanique ChEBI
ácido ciánico ChEBI
acidum cyanicum ChEBI
Cyanic acid KEGG COMPOUND
Cyansäure ChEBI
HOCN IUPAC
Zyansäure ChEBI
Manual Xrefs Databases
0NM PDBeChem
525 ChemSpider
C01417 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
1732479 Beilstein Registry Number Beilstein
420-05-3 CAS Registry Number KEGG COMPOUND
420-05-3 CAS Registry Number ChemIDplus
420-05-3 CAS Registry Number NIST Chemistry WebBook
839 Gmelin Registry Number Gmelin
Citations
Mladenović M, Elhiyani M, Lewerenz M (2009)
Electric and magnetic properties of the four most stable CHNO isomers from ab initio CCSD(T) studies.
The Journal of chemical physics 131, 034302 [PubMed:19624192]
[show Abstract]
Matsumura M, Kojima T (2003)
Elution and decomposition of cyanide in soil contaminated with various cyanocompounds.
Journal of hazardous materials 97, 99-110 [PubMed:12573832]
[show Abstract]
Tsipis CA, Karipidis PA (2003)
Mechanism of a chemical classic: quantum chemical investigation of the autocatalyzed reaction of the serendipitous wöhler synthesis of urea.
Journal of the American Chemical Society 125, 2307-2318 [PubMed:12590561]
[show Abstract]
Oimomi M, Ishikawa K, Kawasaki T, Kubota S, Yoshimura Y, Baba S (1984)
Carbamylation of hemoglobin in renal failure and clinical aspects.
Metabolism: clinical and experimental 33, 999-1002 [PubMed:6493050]
[show Abstract]
Garner MH, Bogardt RA, Gurd FR (1975)
Determination of the pK values for the alpha-amino groups of human hemoglobin.
The Journal of biological chemistry 250, 4398-4404 [PubMed:237898]
[show Abstract]
Renner G (1974)
[Biochemical reactions of cyanic acid as the basis for therapy of cyanic acid poisoning].
Deutsche medizinische Wochenschrift (1946) 99, 1693-1695 [PubMed:4368066]
DIRNHUBER P, SCHUTZ F (1947)
Distillation of cyanic acid as evidence for the presence of cyanate in red cells.
The Biochemical journal 41, liv [PubMed:20340793]
WERNER AE, GRAY J (1947)
Study of the polymerisation of cyanic acid, with special reference to dicyanic acid.
The scientific proceedings of the Royal Dublin Society. Royal Dublin Society 24, 209-214 [PubMed:20261792]
WERNER AE (1947)
Studies on ureides; constitution of Hallwachs' acid; a new copolymer of cyanamide and cyanic acid.
The scientific proceedings of the Royal Dublin Society. Royal Dublin Society 24, 199-208 [PubMed:20261791]
Holmes BE, Watchorn E (1929)
Studies in the metabolism of tissues growing in vitro: Cyanic acid as a possible precursor of the ammonia and urea formed by embryo kidney tissue.
The Biochemical journal 23, 199-205 [PubMed:16744204]
Fearon WR, Dockeray GC (1926)
A Note on the Hydrolysis of Cyanic Acid.
The Biochemical journal 20, 13-16 [PubMed:16743625]
Last Modified
04 March 2022