Weight | 331.202 g/mol |
---|---|
Formula | C17H12Cl2N2O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 3 |
Rotatable Bonds | 3 |
FENARIMOL (60168-88-9)
alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethanol · Rubigan-4 · Rubigan 12 RC
Score:
#3011 in Biology
,
#3762 in Chemistry
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- An energy-dependent efflux mechanism for fenarimol in a wild-type strain and fenarimol-resistant mutants of Aspergillus nidulans (Pesticide Biochemistry and Physiology, 1980)
- Daphnia magna and ecotoxicogenomics: gene expression profiles of the anti-ecdysteroidal fungicide fenarimol using energy-, molting- and life stage-related cDNA libraries. (Chemosphere, 2007)
- Mechanism of resistance to fenarimol in Aspergillus nidulans (Pesticide Biochemistry and Physiology, 1979)
- Occurrence of resistance in Uncinula necator to triadimefon, myclobutanil, and fenarimol in California grapevines (Plant Disease, 1996)
- Antiandrogenic effects in short-term in vivo studies of the fungicide fenarimol. (Toxicology, 2005)
- Inhibition of central nervous system aromatase activity: A mechanism for fenarimol-induced infertility in the male rat (Toxicology and Applied Pharmacology, 1987)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethanol
- Rubigan-4
- Rubigan 12 RC
-
SMILESC1=CC=C(C(=C1)C(C2=CC=C(C=C2)Cl)(C3=CN=CN=C3)O)Cl
-
InChIKeyNHOWDZOIZKMVAI-UHFFFAOYSA-N
- Pubchem - FENARIMOL
- Wikipedia - fenarimol
Fenarimol, sold under the tradenames Bloc, Rimidin and Rubigan, is a fungicide which acts against rusts, blackspot and mildew fungi. It is used on ornamental plants, trees, lawns, tomatoes, peppers, eggplants, cucumbers and melons. It is mainly used to control powdery mildew.
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Synthesis
CHLOROBENZENE
+
Reactant
(Friedel-Crafts alkylation)
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