CHEBI:81960 - dodemorph

ChEBI IDCHEBI:81960
ChEBI Namedodemorph
Stars
DefinitionA member of the class of morpholines that is 2,6-dimethylmorpholine in which the hydrogen attached to the nitrogen is replaced by a cyclododecyl group. It is a fungicide used for the control of powdery mildew, particularly in rose culture.
Last Modified24 July 2015
DownloadsMolfile
FormulaC18H35NO
Net Charge0
Average Mass281.484
Monoisotopic Mass281.27186
SMILESCC1CN(C2CCCCCCCCCCC2)CC(C)O1
InChIInChI=1S/C18H35NO/c1-16-14-19(15-17(2)20-16)18-12-10-8-6-4-3-5-7-9-11-13-18/h16-18H,3-15H2,1-2H3
InChIKeyJMXKCYUTURMERF-UHFFFAOYSA-N
Roles Classification
Chemical Role:
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
antifungal agrochemical  Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
sterol biosynthesis inhibitor  Any compound that inhibits the biosynthesis of any sterol.
fungicide  A substance used to destroy fungal pests.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
antifungal agent  An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce.
Applications:
antifungal agrochemical  Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
fungicide  A substance used to destroy fungal pests.
ChEBI Ontology
Outgoing Relation(s)
dodemorph (CHEBI:81960) has role antifungal agrochemical (CHEBI:86328)
dodemorph (CHEBI:81960) has role sterol biosynthesis inhibitor (CHEBI:83317)
dodemorph (CHEBI:81960) is a macrocycle (CHEBI:51026)
dodemorph (CHEBI:81960) is a morpholine fungicide (CHEBI:87134)
dodemorph (CHEBI:81960) is a tertiary amino compound (CHEBI:50996)
IUPAC Name 
4-cyclododecyl-2,6-dimethylmorpholine
Synonym  Source
dodémorpheChemIDplus
Brand Names  Source
MeltatoxChemIDplus
DoazineChemIDplus
Manual XrefsDatabases
C18786KEGG COMPOUND
dodemorphAlan Wood's Pesticides
BE614214Patent
US3686399Patent
262PPDB
Registry NumbersSources
Reaxys:511312Reaxys
CAS:1593-77-7KEGG COMPOUND
CAS:1593-77-7ChemIDplus
Citations