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2.4.6- trichlorophenyl- ether

Herbicide combinations developed for paddy rice are Satum-S , containing benthiocarb and simetryne, and Satum-M , containing benthiocarb and 4-nitro-phenyl 2,4-6-trichlorophenyl ether. [Pg.646]

MA copolymerization, 667 Allyl 3-sulfonyl ether, MA copolymerization, 537 Allyl tetradecyl ether, MA copolymerization, 671 Allyl 1,3,5-trichlorophenyl ether, MA copolymerization, 663 Allyl 2,4,6-trichlorophenyl ether, MA copolymerizastion, 665... [Pg.821]

Haloprogin. 3-Iodo-2-propynyl 2,4,5-trichlorophenyl ether, is an almost iasoluble antifungal for topical use, available ia the United... [Pg.255]

Haloprogin Haloprogin, 3-iodo-2-propinyl-2,4,5-trichlorophenyl ether (35.4.11), is synthesized by an iodide substitution using a mixture of iodine and potassium iodide and a cupric derivative of 2,4,5-trichlorophenylpropargyl ether (35.4.10), which is synthesized by a standard method from propargyl bromide and 2,4,5-trichlorophenol in the presence of sodium hydroxide [65-67]. [Pg.545]

Thus 4-chlorophenyl 2,4,5-trichlorophenyl ether (48, Scheme 7) produced 4% of a mixture of the dibenzofurans 49 and 50. Only in the case of 2,3,4-trichlorophenyl 2,3,4,5,6-pentai hlorophenyl ether was production of dibenzofurans by formal loss of o,o -chlorine detected. Neither product was identified, but one is presumably the expected product, 1,2,3,4,8,9-hexachloro-dibenzofuran, and the other must be due to a rearrangement. Chlorination of diphenyl ether in the gas phase is unusual. At 300°C the major product is 4-chlorophenyl phenyl ether, as in the liquid phase, but as the temperature is increased (400-500°C), the amount of 4-chlorophenyl phenyl ether decreases at the expense of 3-chlorophenyl phenyl ether, and dibenzofuran is also produced. ... [Pg.18]

C8H18N203S L-buthionine-(S,R)-sulfoximine 83730-53-4 25.00 1.1249 2 15787 C9H4CI3IO 3-iodo-2-propynyl-2,4,5-trichlorophenyl ether 777-11-7 25.00 1.9350 2... [Pg.241]

Iodo-2-prop3myl 2, 4, 5-trichlorophenyl ether 2, 4, 5-Trichlorophenyl y-iodopropai l... [Pg.255]

CAS 3380-34-5 El NECS/ELINCS 222-182-2 Synonyms 5-Chloro-2-(2,4-dichlorophenoxy) phenol 2 -Hydroxy-2,4,4 -trichlorophenyl ether 2,4,4 -Trichloro-2 -hydroxydiphenyl ether... [Pg.4496]

Hydroxytoluene a-Hydroxytoluene. See Benzyl alcohol Hydroxytoluene, butylated. See BHT P-Hydroxytricarballylic acid. See Citric acid 2 -Hydroxy-2A4 -trichlorophenyl ether See Triclosan 41-Hydroxy-3,6,9,12,15,18,21,24,27,30,33,36,39-tridecaoxahentetracont-1-yl octadecanoate. See PEG-14 stearate... [Pg.2162]

The purification of chlornitrofen and the reduced metabolite, 2,4,6-trichlorophenyl 4-aminophenyl ether (CNP-NH2) in brown rice and vegetables was investigated. ... [Pg.455]

It is apparent from extensive reviews of the induction of monooxygenase activity by xenobiotics that many compounds other than methylenedioxyphenyl compounds have the same effect. It may be that any synergist that functions by inhibiting microsomal monooxygenase activity could also induce this activity on longer exposure, resulting in a biphasic curve as described previously for methylenedioxyphenyl compounds. This curve has been demonstrated for NIA 16824 (2-methylpropyl-2-propynyl phenylphosphonate) and WL 19255 (5,6-dichloro-l,2,3-benzothiadiazole), although the results were less marked with R05-8019 [2,(2,4,5-trichlorophenyl)-propynyl ether] and MGK 264 [A-(2-ethylhexyl)-5-norbomene-2,3-dicarboximide],... [Pg.199]

In addition to the incineration processes, herbicides, CNP (2,4, 6-trichlorophenyl-4 -nitrophenyl ether) and PCP (pentachlorophenol) usage was reported as the major source of dioxins, especially during the late 1960s 1970s. While CNP contained particular non-toxic dioxin congeners such as 1,3,6,8-TeCDD and 1,3,7,9-TeCDD (Yamagishi et al.,... [Pg.21]

Trichlorophenyl 4-( -octyloxy) benzoate was then obtained from 4-( -octyloxy) benzoic acid and 2,4,5-trichlorophenol using TV -dicyclohex-ylcarbodiimide in ether. The reacylation of FR179642 was then carried out using the 2,4,5-trichlorophenoyl active ester to yield FR131535. [Pg.419]


See other pages where 2.4.6- trichlorophenyl- ether is mentioned: [Pg.911]    [Pg.510]    [Pg.209]    [Pg.911]    [Pg.510]    [Pg.209]    [Pg.2149]    [Pg.244]    [Pg.753]    [Pg.753]    [Pg.386]    [Pg.1201]    [Pg.1201]    [Pg.1201]    [Pg.1201]    [Pg.1202]    [Pg.196]    [Pg.138]    [Pg.244]    [Pg.105]    [Pg.1817]    [Pg.1817]    [Pg.244]    [Pg.214]    [Pg.17]    [Pg.401]    [Pg.725]    [Pg.975]    [Pg.976]    [Pg.345]    [Pg.753]    [Pg.753]   
See also in sourсe #XX -- [ Pg.364 ]




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3.4.5- Trichlorophenyl

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