CHEBI:34692 - dicofol

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ChEBI Name dicofol
ChEBI ID CHEBI:34692
Definition A tertiary alcohol that is DDT in which the benzylic hydrogen has been replaced by a hydroxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C14H9Cl5O
Net Charge 0
Average Mass 370.48416
Monoisotopic Mass 367.90960
InChI InChI=1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H
InChIKey UOAMTSKGCBMZTC-UHFFFAOYSA-N
SMILES OC(c1ccc(Cl)cc1)(c1ccc(Cl)cc1)C(Cl)(Cl)Cl
Roles Classification
Application(s): acaricide
A substance used to destroy pests of the subclass Acari (mites and ticks).
(via organochlorine acaricide )
pesticide
Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
(via organochlorine pesticide )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing dicofol (CHEBI:34692) has functional parent DDT (CHEBI:16130)
dicofol (CHEBI:34692) is a monochlorobenzenes (CHEBI:83403)
dicofol (CHEBI:34692) is a organochlorine acaricide (CHEBI:38657)
dicofol (CHEBI:34692) is a tertiary alcohol (CHEBI:26878)
IUPAC Name
2,2,2-trichloro-1,1-bis(4-chlorophenyl)ethanol
Synonyms Sources
1,1-bis(4-chlorophenyl)-2,2,2-trichloroethanol ChemIDplus
1,1-bis(p-chlorophenyl)-2,2,2-trichloroethanol ChemIDplus
2,2,2-trichloro-1,1-bis(p-chlorophenyl)ethanol ChemIDplus
4,4'-dichloro-α-(trichloromethyl)benzhydrol NIST Chemistry WebBook
4-chloro-α-(4-chlorophenyl)-α-(trichloromethyl)benzenemethanol NIST Chemistry WebBook
Acarin ChemIDplus
di-(p-chlorophenyl)trichloromethylcarbinol ChemIDplus
Dicofol KEGG COMPOUND
DTMC NIST Chemistry WebBook
Kelthane KEGG COMPOUND
Mitigan ChemIDplus
p,p-dicofol NIST Chemistry WebBook
Manual Xrefs Databases
223 PPDB
C14301 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
115-32-2 CAS Registry Number NIST Chemistry WebBook
115-32-2 CAS Registry Number ChemIDplus
1886299 Beilstein Registry Number ChemIDplus
Last Modified
24 October 2014