5-(2-Chlor-4'-fluorbenzhydryl)-4-hydroxypyrimidin

Bezeichnung:5-(2-Chlor-4'-fluorbenzhydryl)-4-hydroxypyrimidin

CAS-Nr63284-71-9

Englisch Name:NUARIMOL

CBNumberCB3375554

SummenformelC17H12ClFN2O

Molgewicht314.74

MOL-Datei63284-71-9.mol

Synonyma

5-(2-Chlor-4'-fluorbenzhydryl)-4-hydroxypyrimidin

5-(2-Chlor-4'-fluorbenzhydryl)-4-hydroxypyrimidin physikalisch-chemischer Eigenschaften

Schmelzpunkt	126°C
Siedepunkt	475.2±40.0 °C(Predicted)
Dichte	1.3255 (estimate)
Dampfdruck	1 x 10^-5 Pa at 23 °C
storage temp.	0-6°C
Löslichkeit	Chloroform (Slightly), Methanol (Slightly)
pka	11.37±0.29(Predicted)
Wasserlöslichkeit	26 mg l^-1 (pH 7) at 25 °C
Farbe	White to Pale Yellow
BRN	6223667
EPA chemische Informationen	Nuarimol (63284-71-9)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-36
S-Sätze:	26
WGK Germany	3
RTECS-Nr.	UV9279700

Gefahreninformationscode (GHS)

NUARIMOL Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36:Reizt die Augen.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Verwenden
Nuarimol is a systemic fungicide with both curative and protective activity. It controls a wide range of pathogenic fungi, e.g. Cercosporella spp., Septoria spp., Ustilago spp., powdery mildews, leaf spot, etc. in cereals (as a foliar spray and as a seed treatment), powdery mildews on pome fruits, stone fruits, vines, cucurbits and other crops and scab on apples.
Verwenden
Nuarimol is used in the preparation of difluoroethyl-containing heterocyclic compounds useful as antiviral agents and fungicides. Also used as a substance in the modelling inhibition of avian aromatase by azole pesticides.
Stoffwechselwegen
Photolytic degradation is the primary dissipation mechanism of nuarimol in the environment. Major degradation reactions observed on plants/soil surfaces and water include hydroxylation of the phenyl groups, oxidation of the carbinol carbon atom, dehalogenation and carbinol dehydroxylation (Scheme 1). The primary metabolic pathway of nuarimol in rats involves mainly aryl hydroxylation (Scheme 2).
Degradation
Nuarimol is stable to hydrolytic degradation when maintained in sterile buffered solutions (pH 3,6 and 9) in the dark at 52 °C (Saunders, 1977). It was readily degraded in distilled water via photolysis. The photolytic DT₅₀ of nuarimol was approximately 1 hour. Numerous photoproducts were observed; however, no structural characterisation information was reported (Zornes and Donoho, 1978).
Nuarimol was extensively photodegraded on solid surfaces. More than 80 photodegradation products were observed when nuarimol was exposed to sunlight on a stainless steel surface for up to 150 hours (Althaus, 1980a). All photoproducts were formed at very low levels (less than 3% each). The structures of 23 photoproducts were identified. An abbreviated photodegradation pathway of nuarimol (based on products accounting for 1% or greater) is presented in Scheme 1. These products were generated from the following reactions: aryl hydroxylation of the chlorophenyl and fluorophenyl moieties (to yield 2, 3), cleavage of the pyrimidine ring and the oxidation of the carbinol carbon atom (4,5) and dehydroxylation of the carbinol moiety (6). Carboxylic acid fragments from the phenyl(7,8,9) and pyrimidine moieties (10), resulting from the cleavage of the parent phenyl and pyrimidine linkages, were also observed.

5-(2-Chlor-4'-fluorbenzhydryl)-4-hydroxypyrimidin Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

63284-71-9, NUARIMOL Verwandte Suche:

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