http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S5463042-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_2baf849d216e689ecc40ccc931a7a7bc
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C205-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-15
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C227-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C201-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-38
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-32
filingDate 1977-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bcdcda2be1e9ebbd7b344a6a4085d6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_17f8c62b3c13fa41090a1bdbaaeb2986
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86ea966b5af0226388fcece3f5838f17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f88a0a6bcc709238ff974d88db26b75
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08833c610d888e60b19c8cc69fc10fda
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_789bed02ec436f3cf6ff94cd3a621e49
publicationDate 1979-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S5463042-A
titleOfInvention Substituted phenylacetic acid and its preparation
abstract NEW MATERIAL:0-(4-Amino-2,6-dichoroanilino)-phenylacetic acid. n USE: Intermediate for 2-(2,6-dichloroanilino) phenylacetic acid. Sodium salt of the 2-(2,60dichloroanilino) phenyl acetic acid has an anti-inflammatory, analogesic, and antipyretic actions and is a drug known as the general name Dichlorophenac sodium. n PROCESS: 1-(4-Amino-2,6-dichlorophenyl) indolinone of formual II is hydrolyzed with an alkali, e.g. sodium hydroxide, etc. to form an alkali metal salt of 0-(4- amino-2,6-dichloroanilino) phenylacetic acid. The alkali metal salt thus obtained is neutralized with an acid, e.g. hydrochloric acid, etc. to form the objective compound of formula I. The starting compound of formula II is obtained from inexpensive 2,6-dichloro-4-nitroaniline of formula III available as an intermediate for azo disperse dyes. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1977-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226581612
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419555698
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559553
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226693463
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7430
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419583338
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1549559
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID999
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14798
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5360545
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4049991
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226395154
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409060395
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419523755
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416129933
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432311414
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154275891
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3033

Total number of triples: 47.