Bi-aromatic compounds and pharmaceutical and cosmetic compositio

Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Cosmetic – antiperspirant – dentifrice

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424 701, 424400, 424422, 424427, 546304, 546329, 549 68, 549 74, 560 13, 560 35, 562427, 562440, 564162, 564245, 514166, 5142312, 5142315, 5142318, 514252, 514255, 514315, 514316, 514317, 514326, 514327, 514331, 514422, 514426, 514438, 514444, 514448, 514461, 514471, 514508, 514514, 514532, 514543, 514557, 514576, 514637, 514726, 514731, 514741, 514562, 514564, 514567, A61K 900

Patent

active

057532397

ABSTRACT:
Bi-aromatic compounds are provided along with methods for their preparation and use.

REFERENCES:
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patent: 4264505 (1981-04-01), Shroff et al.
Chemical Abstracts, vol. 92, No. 9, Mar. 1980, Abstract No. 76036M, Albu, "Cumylphenol Derivatives, III. Synthesis and Electronic Spectra Ofsome Cumylphenol-Derived Arylazomethines".
Chemical Abstracts, vol. 77, No. 17, Oct. 1972, Abstract No. 113925, Bruk et al, "Screened Phenols. VI. Azomethines, Derivatives of 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde".
Chemical Abstracts, vol. 111, No. 7, Aug. 1989, Abstract No. 56768J, Ivakhnenko et al, "Synthesis of Sterically Hindered Diarylamidine Phenols and Properties of Radicals Formed From Them".
French Search Report of FR 91 05883.
Vila et al, Synth. React, Inorg. Met. -Org. Chem. 1988 18(1)47-67 cited in Chem. Abstract vol. 110:213030M vol. 110, 1989.
Ivakhnenko et al, Zh. Org. Khim. 1989 (25(2)357-367 cited in Chem. Abstract vol. 111, 1989, p. 674 111:56768.
Makovec et al, J.Med. Chem. 35(20) 3633-40 1992 cited in Chem. Abstract vol. 117(17) 170914C.
Kato et al. WO 9111994 Aug. 22, 1991, cited in Chem. Abstract 116(12):128356b.
Bruk, CA vol. 77, 1972 113922k p. 409 Screened phenols VI Azomethines.
Manda, CA vol. 82, 1975 42507M p. 367 synthesis & oxidation of 4-(N-arylmethylidenea ino-2,6-di-tert butylphenols.

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