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M-Cresylic

Since the Fries rearrangement is a equilibrium reaction, the reverse reaction may be used preparatively under appropriate experimental conditions. An instructive example, which shows how the regioselectivity depends on the reaction temperature, is the rearrangement of m-cresyl acetate 8. At high temperatures the ortho-product 9 is formed, while below 100°C the para-derivative 10 is formed ... [Pg.128]

Fecal excretion may gain relative importance as an excretory route for tri-/xrra-cresyl phosphate as doses approach levels of 100 mg/kg (Kurebayashi et al. 1985 NTP 1988). Fecal excretion of tn-m-cresyl phosphate appears to be predominant in rats even at a dose level of 200 mg/kg (NTP 1988). [Pg.177]

Trade names o-cresylic acid No data p-cresylic acid m-cresylic acid cresylic acid CAS 1989 HSDB 1989... [Pg.72]

Vennin, Burlot Lecorche (Ref 5, p 454) were of the opinion that Ecrasite was Ammonium Trinitxo-m-cresylate, which they called Le cresylate d ammoniaque or simply Cresylate. [Pg.651]

Note Here is evidently an errot and compn must be PA 60 Ammonium Trinitro-m-cresylate (called in French the "Cresylite )... [Pg.651]

Accdg to Stettbacher (Refs 6 8) Austrian expl Ekrosit did not contain any Ammonium Trinitro-m-cresylate but was either straight... [Pg.651]

Phenyl n-propyl et.her. Phenyl n-butyl ether o-Cresyl methyl ether (1) m-Cresyl methyl ether. p-Cresyl methyl ether. o-Cresyl ethyl ether m-Cresyl ethyl ether p-Cresyl ethyl ether Benzyl methyl ether Benzyl ethyl ether Methyl a-naphthyl ether Methyl p-naphthyl ether Ethyl a-naphthyl ether Ethyl p-naphthyl ether Benzyl a-naphthyl ether Benzyl P-naphthyl ether o-Methoxydiphenyl p-Methoxydiphenyl. o-Chloroanisole. m-Chloroanisole. p-Chloroanisolc o-Bromoanisole m-Bromoanisole. p-Bromoanisole. o-Iodoanisole m-Iodoanisole p-Iodoanisole o-Nitroanisole... [Pg.673]

Cresyl acetate p-Cresyl acetate m-Cresyl acetate Guaiacol acetate Thymyl acetate Carvacryl acetate Resorcinol diacetate Eugenol acetate... [Pg.1359]

Mw = 9300, Mw/Mn = 5.07). The poly (p-hydroxy styrene) was PHP-6817-24, obtained from Marusen Oil Co. (Mn = 3900, Mw = 10200, Mw/Mn = 2.62). Kodak micro positive developer 934 (934 developer) (predominantly tetramethyl ammonium hydroxide in water) was used at various dilutions with deionized water. M-cresyl naphthalene diazo-quinone sulfonate was prepsured by a pyridine catalyzed condensation of m-cresol with naphthalene diazoguinone sulfonyl chloride. [Pg.248]

SYNS 3-CRESOL m-CRESYLIC ACIDQ 1-HYDROXY-3-METHYLBENZENE O m-HYDROXY-TOLUENE m-KRESOL m-METHYLPHENOL 3-METHYLPHENOL m-OXYTOLUENE RCRA WASTE NUMBER U052 m-TOLUOL... [Pg.391]

SYNS CARBAMIC ACID, METHYL-, 3-METHYLPHEN-YL ESTER (9CI) CARBAMIC ACID, METHYE, 3-TOLYL ESTER m-CRESYL METHYLCARBAMATE DICRES-YL DICRESYL N-METHYLCARBAMATE DRC 3341... [Pg.908]

Synonym m-cresylic acid, 1-hydroxy-3-methylbenzene, 3-hydroxytoluene, m-hydroxytoluene, 3-methylphenol, m-methy Iphenol, 3-cresol... [Pg.551]

FIGURE 15.1.4.1.7.1a Logarithm of vapor pressure versus reciprocal temperature for tr/s(m-cresyl) phosphate. [Pg.904]

See other pages where M-Cresylic is mentioned: [Pg.673]    [Pg.673]    [Pg.789]    [Pg.789]    [Pg.790]    [Pg.673]    [Pg.673]    [Pg.789]    [Pg.789]    [Pg.790]    [Pg.298]    [Pg.83]    [Pg.83]    [Pg.147]    [Pg.548]    [Pg.789]    [Pg.789]    [Pg.790]    [Pg.419]    [Pg.811]    [Pg.610]    [Pg.1360]    [Pg.1360]    [Pg.1397]    [Pg.1397]    [Pg.1360]    [Pg.1360]    [Pg.1397]    [Pg.1397]    [Pg.548]    [Pg.1595]    [Pg.83]    [Pg.147]    [Pg.284]    [Pg.540]   
See also in sourсe #XX -- [ Pg.209 ]



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M-Cresyl acetate

M-Cresylic acid

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