The alpha-Haloalkyl Ethers

Summers, Lawrence H.

doi:10.1021/cr50002a003

Cited by 78 publications

(9 citation statements)

References 76 publications

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“…1-Alkoxymethyl-2,4,5-triha1oimidazoles were prepared by the reaction of 2,4,5-triha10imidazoles 4 ) with ha10methyl ethers 5 ) in the presence of a base. The structure of each compound was confirmed by IR and IH-NMR spectroscopy, as well as by elemental analysis.…”

Section: Methodsmentioning

confidence: 99%

Insecticidal Activity of Novel Trihaloimidazole Derivatives against a Wild Colony of German Cockroaches (Blattella germanicd)

Tomioka

Yano

Takada

et al. 1991

Agricultural and Biological Chemistry

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Section: Methodsmentioning

confidence: 99%

Insecticidal Activity of Novel Trihaloimidazole Derivatives against a Wild Colony of German Cockroaches (Blattella germanicd)

Tomioka

Yano

Takada

et al. 1991

Agricultural and Biological Chemistry

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“…They can be synthesized by direct chlorination of the appropriate ethers or by the sulfuric acid process (see Chapter 3); however, the former method is not used on a commercial scale. Chloroalkyl ethers can also be produced by reacting aldehydes with hydrogen chloride [43]:…”

Section: Chloroalkyl Ethersmentioning

confidence: 99%

Ethers, Aliphatic

Sakuth¹,

Mensing²,

Schuler³

et al. 2010

Ullmann's Encyclopedia of Industrial Chemistry

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The article contains sections titled: 1. Introduction 2. Properties 2.1. Physical Properties 2.2. Chemical Properties 2.2.1 General Aspects 2.2.2 Peroxide Formation Tendency of Ethers 3. Synthesis 4. Individual Aliphatic Ethers 4.1. Diethyl Ether 4.2. Diisopropyl Ether 4.3. Other Aliphatic Ethers 4.3.1. Di‐ n ‐propyl Ether 4.3.2. Di‐ n ‐butyl Ether 4.3.3. Diamyl Ether 4.4. Chloroalkyl Ethers 4.4.1. Bis(chloromethyl) Ether 4.4.2. Bis(2‐chloroethyl) Ether 4.4.3. Bis(2‐chloroisopropyl) Ether 5. Toxicology

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“…Verschiedene anderefur die Laborentgiftung weniger bedeutsame -Methoden werden beschrieben [34], z.B. die eisenkatalysierte Hydrolyse [%I, die Reaktionen mit 2-Hydrazono-2,3dihydro-3-methylbenzthiazol-hydrochlorid, 4-Pyridinaldehyd-2benzthiazolyl-hydrazon [36] und Kupferdiethylmalonat [37], die Addition an Olefine [38], die Chlormethylierung von Xylen [39]…”

Section: Chloretherunclassified

Chemische Entgiftung wichtiger organischer Cancerogene im Laboratorium

Martinetz

1986

Zeitschrift fuer Chemie

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Diverse classes of chemicals can induce cancer in animals and men. A review is given on laboratory detoxification of some types of chemical carcinogens and the basic principles involved in laboratory safety. No general techniques exist for the decontamination of such substances. Effective methods for the destruction of aflatoxins, aromatic amines, chloroethers, hydrazines, N‐nitrosamines and ‐amides, polycyclic aromatic hydrocarbons and some single substances (e.g. yperites, selected nitro compounds, azides, triazenes, dioxins, and captane, mercapto purine, thioguanine) in laboratory wastes are described. The methods preferred by the International Agency for Research on Cancer (Lyon) are especially considered. Destruction techniques for chemical carcinogens must be efficient, complete, irreversible, rapid, reproducible, easy to perform, and the product of detoxification must be free of mutagenic and/or carcinogenic activity.

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The alpha-Haloalkyl Ethers

Cited by 78 publications

References 76 publications

Insecticidal Activity of Novel Trihaloimidazole Derivatives against a Wild Colony of German Cockroaches (Blattella germanicd)

Insecticidal Activity of Novel Trihaloimidazole Derivatives against a Wild Colony of German Cockroaches (Blattella germanicd)

Ethers, Aliphatic

Chemische Entgiftung wichtiger organischer Cancerogene im Laboratorium

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