http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-4234627-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D211-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D295-155
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09K19-3441
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-34
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D211-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-155
filingDate 1992-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_612f6a806de257f36718c0f27206eea6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_da98f1dbd4e4c3974ccb035eec9e1c6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0540c5163cf547db00a31727724170c0
publicationDate 1994-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-4234627-A1
titleOfInvention (3-fluorophenyl) piperidines and piperazines
abstract New (3-fluorophenyl)-piperidines and -piperazines are of formula (I), where R1=1-18C alk(en)yl, opt. with halogen substit(s). or a CN substit. in which 1 or 2 non-adjacent CH2 gps. may be replaced by -O-, -CO-O-, -O-CO- or -S-; A1=1,4-phenylene, opt. with 1-2F substits., in which 1 or 2 CH gps. may be replaced by N; 1,4-cyclohexylene, opt. with a CN substit., in which 1 or 2 CH2 gps. may be replaced by O or S; thiadiazole-2,5-diyl; or 1,4-bicyclo(2,2,2)- octylene; L1-3=H or F; Z1-2=-CO-O-, -O-CO-, -CH2O-, -OCH2-, -CH2CH2-, -C=C- or a single bond; W=CH or N; X=CN, NCS, halogen or a 1-8C alk(en)yl or alk(enyl)oxy gp., opt. with F and/or Cl substit(s)., in which 1 CH2 gp. may be replaced by CO; and m and n = 0, 1 or 2. USE/ADVANTAGE - Cpds. with a 1-(3'-fluoro- or 3',5'-difluoro-phenyl)-piperidin-1,4'-diyl or -piperazin-1,4'-diyl gp., esp. (I) are used in liq. crystal (LC) media, which are used in electrooptical displays (claimed). (I) are esp. useful in twisted cell, guest-host, deformation aligned phase or dynamic scattering type LCDs. (I) are stable LC or mesogenic cpds. with relatively low viscosity and high dielectric anisotropy. Media contg. (I) are stable and have relatively low viscosity, a wide mesophase range, favourable optical and dielectric anisotropy and very good low temp. properties.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101747905-B
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priorityDate 1992-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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