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Fenazaquin

CAS 120928-09-8C20H22N2OMW 306.4

Fenazaquin (CAS 120928-09-8) — formula C20H22N2O, molecular weight 306.4.

Product Overview

CAS Number120928-09-8
Molecular FormulaC20H22N2O
Molecular Weight306.4
Melting Point77.5-80 °C
LogPlog Kow = 5.51 at 20 °C
ApplicationsUses: For fenazaquin (USEPA, OPP Pesticide Code: 044501) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Miticide and insecticide, Acaracide, Use Classification: Acaricides, Insecticides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: Fenazaquin is produced by reaction of 4-hydroxyquinazoline with phosphite and chlorine, and treating the resulting haloquinazoline with 4-tert-butylphenylethanol., Formulations, Preparations: Emulsifiable concentrate, suspension concentrate., Fenazaquin Technical (Gowan Company, LLC) Fenazaquin 99.4%, GWN-1708 Miticide, Insecticide (Gowan Company, LLC) Fenazaquin 18.79%, General Manufacturing Information: The majority of usage is in Europe (>80%), The WHO Recommended Classification of Pesticides by Hazard identifies fenazaquin (technical grade) as Class II: moderately hazardous, Main Use: acaracide.

Applications

Documented applications: Uses: For fenazaquin (USEPA, OPP Pesticide Code: 044501) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Miticide and insecticide, Acaracide, Use Classification: Acaricides, Insecticides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: Fenazaquin is produced by reaction of 4-hydroxyquinazoline with phosphite and chlorine, and treating the resulting haloquinazoline with 4-tert-butylphenylethanol., Formulations, Preparations: Emulsifiable concentrate, suspension concentrate., Fenazaquin Technical (Gowan Company, LLC) Fenazaquin 99.4%, GWN-1708 Miticide, Insecticide (Gowan Company, LLC) Fenazaquin 18.79%, General Manufacturing Information: The majority of usage is in Europe (>80%), The WHO Recommended Classification of Pesticides by Hazard identifies fenazaquin (technical grade) as Class II: moderately hazardous, Main Use: acaracide..

Technical Profile

What this product is

Fenazaquin is a chemical compound with CAS registry number 120928-09-8 and molecular formula C20H22N2O (molecular weight 306.4).

Identification

CAS number: 120928-09-8

Its molecular formula C20H22N2O comprises 20 C, 22 H, 2 N, 1 O atoms.

Also known as: Fenazaquin · 喹草酮

Frequently Asked Questions

What is the CAS number of Fenazaquin?

The CAS registry number of Fenazaquin is 120928-09-8.

What is the molecular formula and molecular weight of Fenazaquin?

Molecular formula C20H22N2O, molecular weight 306.4.

What other names is Fenazaquin known by?

It is also registered under: Fenazaquin, 喹草酮.

What are the documented applications of Fenazaquin?

Recorded applications: Uses: For fenazaquin (USEPA, OPP Pesticide Code: 044501) ACTIVE products with label matches., SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Miticide and insecticide, Acaracide, Use Classification: Acaricides, Insecticides, Environmental transformation -> Pesticides (parent, predecessor), Methods of Manufacturing: Fenazaquin is produced by reaction of 4-hydroxyquinazoline with phosphite and chlorine, and treating the resulting haloquinazoline with 4-tert-butylphenylethanol., Formulations, Preparations: Emulsifiable concentrate, suspension concentrate., Fenazaquin Technical (Gowan Company, LLC) Fenazaquin 99.4%, GWN-1708 Miticide, Insecticide (Gowan Company, LLC) Fenazaquin 18.79%, General Manufacturing Information: The majority of usage is in Europe (>80%), The WHO Recommended Classification of Pesticides by Hazard identifies fenazaquin (technical grade) as Class II: moderately hazardous, Main Use: acaracide..

PubChem Public Data

Independent reference data for Fenazaquin (CAS 120928-09-8), compiled from public chemistry databases.

Registry identifiers across databases

CAS Registry Number120928-09-8
PubChem CID86356
Molecular formulaC20H22N2O
IUPAC name4-[2-(4-tert-butylphenyl)ethoxy]quinazoline
UNII (FDA)DK5Q534WEE

Computed descriptors

Molecular Weight306.4
XLogP35.7
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count5
Exact Mass306.173213330
Monoisotopic Mass306.173213330
Topological Polar Surface Area35
Heavy Atom Count23

Physicochemical values on record

Melting Point77.5-80 °C
Density1.16
Vapor Pressure3.4X10-3 mPa /2.55X10-8 mm Hg/ at 25 °C
LogPlog Kow = 5.51 at 20 °C
LogP4.91
Dissociation ConstantspKa = 2.44

Documented uses on record

    Fenazaquin is produced by reaction of 4-hydroxyquinazoline with phosphite and chlorine, and treating the resulting haloquinazoline with 4-tert-butylphenylethanol.The majority of usage is in Europe (>80%)

    Synonyms and trade names

    Fenazaquin; 120928-09-8; Magister; 4-[2-(4-tert-butylphenyl)ethoxy]quinazoline; 4-tert-Butylphenethylquinazolin-4-yl ether; DTXSID4040476; DK5Q534WEE; 4-((4-(1,1-Dimethylethyl)phenyl)ethoxy)quinazoline; 4-tert-butylphenethyl quinazolin-4-yl ether; Quinazoline, 4-(2-(4-(1,1-dimethylethyl)phenyl)ethoxy)-; DTXCID2020476; CHEBI:38593; DE-436; EL-436; 4-(2-(4-(1,1-Dimethylethyl)phenyl)ethoxy)quinazoline; 4-(2-(4-tert-butylphenyl)ethoxy)quinazoline

    GHS hazard classification

    Reported hazard statementsH301, H332, H400, H410

    H301: Toxic if swallowed [Danger Acute toxicity, oral]

    H332: Harmful if inhaled [Warning Acute toxicity, inhalation]

    What the public record says

    Fenazaquin · CAS 120928-09-8 · C20H22N2O. UNII DK5Q534WEE. Melting Point: 77.5-80 °C; Density: 1.16; Vapor Pressure: 3.4X10-3 mPa /2.55X10-8 mm Hg/ at 25 °C.

    Physical description and handling notes

    Source: PubChem / Wikidata; the batch COA governs where values differ.

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