1.
    发明专利
    未知

    公开(公告)号:DE3855862D1

    公开(公告)日:1997-05-15

    申请号:DE3855862

    申请日:1988-12-21

    Applicant: HOECHST AG

    Abstract: The 1-substituted piperidine-4-carboxylic esters of the formula (I) … … are liquid-crystalline and exhibit in particular Sc or SC phases. In this formula, R or R is a radical of the formula (II) … … in which the rings are aromatic, heteroaromatic or cycloaliphatic molecular building blocks which may have hetero atoms, such as 1,4-phenylene, pyrimidine-2,5-diyl or trans-1,4-cyclohexylene, which are linked via a single bond (where n, p is zero) or via functional groups Z1, Z2 such as CO-O or CH2-O and in which k, n, m, p, q are zero or 1, k + m + p being at least 1 and p being zero if m is zero. The other radical R or R is a substituted or unsubstituted straight- chain or branched alkyl group having 1 to 20 carbon atoms, X1 denotes O, S, phenyleneoxy or CH2 and X2 denotes O or phenyleneoxy.

    3.
    发明专利
    未知

    公开(公告)号:DE3506435A1

    公开(公告)日:1986-08-28

    申请号:DE3506435

    申请日:1985-02-23

    Applicant: HOECHST AG

    Abstract: Method and composition for a ketosultam of the general formula in which R1 and R2 are identical or different and each denote hydrogen, (C1 to C8)-alkyl, which is optionally substituted by one or several halogen atoms, hydroxy groups, cyano groups or (C1 to C4)-alkoxy groups, or phenyl, R3 denotes hydrogen or a (C1 to C4)-alkyl group or (C1 to C4)-alkoxy group, n is a number from 1 to 4, or R1, R2 and R3, together with the corresponding aminophenyl group, denote julolidinyl or N-(C1 to C3)-alkylcarbazol-3-yl. The compounds are used in the preparation of sensitizers and dyes.

    10.
    发明专利
    未知

    公开(公告)号:DE3531788A1

    公开(公告)日:1987-03-12

    申请号:DE3531788

    申请日:1985-09-06

    Applicant: HOECHST AG

    Abstract: The invention relates to new 3-halogenoacetonesulfonamides of the formula X-CH2-CO-CH2-SO2NH2 in which X=F, Cl, Br or I, and to the preparation and use thereof. The preparation of the bromine compound according to the invention is effected by reacting acetonesulfonamide with bromine in aqueous solution. The fluorine, chlorine or iodine compound is prepared by reacting the bromine compound with a fluoride, chloride or iodide in an aprotic solvent. The compounds according to the invention can be used for the preparation of azo dyestuffs, plant protection agents, pharmaceuticals and textile auxiliaries.

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