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CHEBI:34393 - 4-chloro-3,5-dimethylphenol

ChEBI IDCHEBI:34393
ChEBI Name4-chloro-3,5-dimethylphenol
Stars
DefinitionA member of the class of phenols that is 3,5-xylenol which is substituted at position 4 by chlorine. It is bactericidal against most Gram-positive bacteria but less effective against Staphylococci and Gram-negative bacteria, and often inactive against Pseudomonas species. It is ineffective against bacterial spores.
Last Modified8 August 2017
DownloadsMolfile
FormulaC8H9ClO
Net Charge0
Average Mass156.612
Monoisotopic Mass156.03419
SMILESCc1cc(O)cc(C)c1Cl
InChIInChI=1S/C8H9ClO/c1-5-3-7(10)4-6(2)8(5)9/h3-4,10H,1-2H3
InChIKeyOSDLLIBGSJNGJE-UHFFFAOYSA-N
Wikipedia
Roles Classification
Biological Role:
disinfectant  An antimicrobial agent that is applied to non-living objects to destroy harmful microorganisms or to inhibit their activity.
Applications:
molluscicide  A substance used to destroy pests of the phylum Mollusca.
antiseptic drug  A substance used locally on humans and other animals to destroy harmful microorganisms or to inhibit their activity (cf. disinfectants, which destroy microorganisms found on non-living objects, and antibiotics, which can be transported through the lymphatic system to destroy bacteria within the body).
ChEBI Ontology
Outgoing Relation(s)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has functional parent 3,5-xylenol (CHEBI:38572)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role antiseptic drug (CHEBI:48218)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role disinfectant (CHEBI:48219)
4-chloro-3,5-dimethylphenol (CHEBI:34393) has role molluscicide (CHEBI:33904)
4-chloro-3,5-dimethylphenol (CHEBI:34393) is a monochlorobenzenes (CHEBI:83403)
4-chloro-3,5-dimethylphenol (CHEBI:34393) is a phenols (CHEBI:33853)
IUPAC Name 
4-chloro-3,5-dimethylphenol
INNs  Source
chloroxylenolChemIDplus
chloroxylénolWHO MedNet
cloroxilenolChemIDplus
chloroxylenolumChemIDplus
Synonyms  Source
chloro-xylenolChemIDplus
2-chloro-5-hydroxy-1,3-dimethylbenzeneChemIDplus
p-chloro-m-xylenolChemIDplus
2-chloro-5-hydroxy-m-xyleneChemIDplus
3,5-dimethyl-4-chlorophenolChemIDplus
4-chloro-m-xylenolChemIDplus
Brand Names  Source
DettolChemIDplus
BenzytolChemIDplus
Manual XrefsDatabases
C14715KEGG COMPOUND
D03473KEGG DRUG
US2350677Patent
LSM-19962LINCS
3094DrugCentral
ChloroxylenolWikipedia
1615PPDB
1615VSDB
Registry NumbersSources
Reaxys:1862539Reaxys
CAS:88-04-0KEGG COMPOUND
CAS:88-04-0ChemIDplus
CAS:88-04-0NIST Chemistry WebBook
Citations