Abstract:
Disclosed are aminomethylenecyanoacetic acid esters and amides of formula (I), in which R?1 and R2¿, independently of each other, are phenyl, naphthyl, biphenyl or a five- or six-membered hetero-aryl group which has one, two or three nitrogen atoms or one oxygen atom or one sulphur atom or one nitrogen and one oxygen atom or one nitrogen and one sulphur atom, and which may be benzannulated, whereby these groups may be substituted by one to three C¿1?-C12-alkyl groups, C1-C12-alkoxy groups, halogen atoms, cyano groups, hydroxy groups or groups of the formulae COOR?3 COR3, CONHR3, OCOR3¿ or NHCOR3, where R3 is C1-C12-alkyl, C5-C8-cycloalkyl or phenyl; X is a C2-C30-alkylene group which may contain non-adjacent oxygen atoms, a C4-C12-alkylene or C4-C12-alkinylene group (the unsaturated bonds not being adjacent to the ester oxygen atoms), a C5-C8-cycloalkylene group or a phenylene group; and Y is O or NH. These compounds can be used as stabilizers for organic materials.
Abstract:
2-Cyanoacrylic esters (I) of alpha , omega -bis(4-hydroxy-2,2,6,6-tetramethylpiperid-1-yl)alkanes or (cyclo)aliphatic polyols of the given formula (I) are new. R , R = the radical of an iso- or heterocyclic ring system with at least one iso- or heteroaromatic ring and ≥ 1 of R and R is not H, n = 2-10, if n = 2, X = a gp. of formula (II), m = 2-8; if n = 3-10, X = the radical of an n-hydric 3-20C (cyclo)aliphatic polyol, opt. with 1 or 2 heteroatoms in the cycloaliphatic gp. and up to 8 non-adjacent O or S atoms or -NH- or 1-4C alkylimino gps. in the aliphatic chain. Also claimed are various materials stabilised against the action of light, O2 and heat with (I).
Abstract:
Proposed is the use, as light-protection agents and stabilizers for non-living organic material, of 3-arylacrylic acid esters (I) in which Ar is an aryl group, which may carry additional substituents, R is an n-valency aliphatic polyol group with up to 20 C-atoms, whereby the carbon chain may be interrupted by up to 9 non-adjacent oxygen atoms, or an n-valency cycloaliphatic polyol group with 5 to 20 C-atoms in which non-adjacent ring carbon atoms may be replaced by oxygen atoms, R and R are hydrogen or C1-C4 alkyl and n is a number from 1 to 10.
Abstract:
Use of 3-amino-2(benzoylamino)acrylic acid esters (I) in which R1 is C1 to C20-alkyl which may be interrupted by one or more non-adjacent O atoms or NR5 groups and may bear one or more hydroxyl groups, C¿2? to C20-alkenyl, C5 to C8-alkenyl, C5 to C8-cycloalkyl or phenyl which may be substituted by one to three C1 to C4-alkyl groups, C1 to C4-alkoxy groups, C1 to C4-alkoxy groups, halogen atoms, hydroxyl groups, phenoxy groups, phenyl radicals, cyano groups or C1 to C4-alkoxy carbonyl groups; R?2¿ is hydrogen or C¿1? to C20-alkyl; R?3¿ is a five or six-component unsaturated or saturated heterocyclic ring with up to three hetero atoms from the group nitrogen, oxygen and sulphur, which is additionally benzannulated and may be substituted by one to three C¿1? to C4-alkyl groups, C1 to C4-alkoxy groups, halogen atoms, hydroxyl groups, phenoxy groups, phenyl radicals, cyano groups or C1 to C4-alkoxycarbonyl groups; R?4¿ is hydrogen, C¿1? to C12-alkyl, C1 to C12-alkoxy, halogen, hydroxyl, phenoxy, phenyl, cyano or a grouping of the formula -CO-OR?5, -CO-R5¿, -O-CO-R5 of -NH-CO-R?5; R5 is C¿1 to C12-alkyl, C5 to C8-cycloalkyl or phenyl; and n is 1 to 3, as stabilisers for organic materials.
Abstract:
Described are cosmetic preparations containing light-screening agents designed to protect the human epidermis against UV light in the region from 280 to 400 nm. The light-screening agents are contained in a carrier compound suitable for cosmetic purposes together with compounds of the formula (I), as given in claim 1, in which R , R and n are as defined in clause 1, which absorb in the UV-B region and are per se prior art for cosmetic preparations, in amounts which are active as photostable UV-A filters.
Abstract:
The present invention pertains to the use of aminovinyl phosphonic acid esters of general formula (I), in which R is cyano, a radical of the formula -CO-OR or a grouping of formula (II), R , R and R are C1 to C20 alkyl, C5 to C8 cycloalkyl, C7 to C18 aralkyl, phenyl or tolyl, R is phenyl, which can be substituted by one to three C1 to C12 alkyl groups, C1 to C12 alkoxy groups, halogen atoms, cyano groups, hydroxyl groups, phenyl groups or groups of formula -CO-OR , -CO-R , -CO-NHR , -O-CO-R or -NH-CO-R , a five- or six-membered unsaturated or saturated heterocyclic ring with up to three heteroatoms from the group of nitrogen, oxygen and sulfur, which ring can also be benzanellated and substituted by one to three C1 to C12 alkyl groups, C1 to C12 alkoxy groups, halogen atoms, cyano groups, hydroxyl groups, phenyl groups, phenoxy groups or C1 to C12 alkoxycarbonyl groups, or a grouping of the formula (III), R is hydrogen or C1 to C12 alkyl, R is hydrogen, C1 to C6 alkyl, formyl, C2 to C6 alkanoyl, C1 to C12 alkoxy, C5 to C6 cycloalkoxy, cyanomethyl, 2-hydroxyethyl, benzyl or a radical of the formula -CR = CH-CO-OR , wherein R is hydrogen, C1 to C6 alkyl or a radical of the formula -CO-OR , and X stands for oxygen or NH, as photoprotective agents and stabilizers for organic material.
Abstract:
A process for producing 2-cyano-3,3-diary acrylic acid esters of general formula (I) in which R and R are hydrogen, C1-C12 alkoxy groups or di-(C1-C4 alkyl) amino groups and R is a C4-C18 alkyl group which may be interrupted by oxygen atoms in the ether function, by the reaction of benzophenonimine of general formula (II) with a cyanic acid ester of general formula (III), in which the reaction is conducted at 20 to 60 DEG C and the ammonia released is continuously removed from the reaction mixture with the aid of a stream of gas or by reducing the pressure to 900 to 100mbar.
Abstract:
Described are 2-cyanoacrylic acid esters (I) in which the groups are defined as follows: R and R are hydrogen or a group with an isocyclic or heterocyclic ring system having at least one iso-aromatic or hetero-aromatic nucleus, whereby one of the groups R and R must be different from hydrogen, n is from 2 to 10, X in the case when n = 2 is a group of the formula (II) in which m is from 2 to 8, X in the case when n > 2 is an n-hydric aliphatic or cycloaliphatic polyol group with 3 to 20 C-atoms, whereby the cycloaliphatic polyol group may include 1 to 2 hetero-atoms and the aliphatic polyol group may include up to 8 non-adjacent oxygen atoms, sulphur atoms, imino groups or C1-C4 alkylimino groups in the carbon chain. Compounds of the formula (I) are suitable for use as light-protection agents.
Abstract:
PCT No. PCT/EP93/00739 Sec. 371 Date Oct. 7, 1994 Sec. 102(e) Date Oct. 7, 1994 PCT Filed Mar. 26, 1993 PCT Pub. No. WO93/20051 PCT Pub. Date Oct. 14, 1993Polyalkylpiperidine-containing acetic acid and 3-aminoacrylic acid derivatives I I where R1 is hydrogen, C1- to C6-alkyl, formyl, C2- to C6-alkanoyl, C1- to C12-alkoxy, C5- to C6-cycloalkoxy, cyanomethyl, hydroxymethyl, 2-hydroxyethyl or a radical of the formula -CR3=CH-CO-OR4, where R3 is hydrogen, C1-to C6-alkyl or a radical of the formula -CO-OR4 and R4 is C1- to C20-alkyl, C5- to C8-cycloalkyl, C7- to C18-aralkyl, phenyl, tolyl or a radical of the formula -(CH2CH2O)nH or -[CH(CH3)CH2O]nH, where n is a number from 1 to 30, X is O, NH or NR6, where R6 is C1- to C12-alkyl, and Y is hydrogen or a group of the formula =CH-NHR7 or =CH-NR6R7, where R7 is phenyl which can be substituted by one to three C1- to C12-alkyl, C1- to C12-alkoxy, halogen, cyano, hydroxyl, phenyl or groups of the formula -CO-OR5, -CO-R5, -CO-NHR5, -O-CO-R5 or -NH-CO-R5, is a 5- or 6-membered unsaturated or saturated heterocyclic ring having up to three hetero atoms from the group comprising nitrogen, oxygen and sulfur, which can additionally be benzo-fused and substituted by one to three C1- to C12-alkyl, C1- to C12-alkoxy, halogen, cyano, hydroxyl, phenyl, phenoxy or C1- to C12-alkoxycarbonyl are described.