http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01151549-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-64
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-113
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07K1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-87
filingDate 1988-11-10^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07de6eb4eec4e1e2d6a943202cd1c890
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4feac6eb020cbfce88aa60c8899fde29
publicationDate 1989-06-14^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01151549-A
titleOfInvention 4-methoxy-2,3,6-trimethylbenzenesulfonyl halide
abstract NEW MATERIAL:4-Methoxy-2,3,6-trimethylbenzenesulfonyl halide. n EXAMPLE: 4-Methoxy-2,3,6-trimethylbenzenesulfonyl chloride. n USE: A guanidino-protecting group. The title compound is introduced to the guanidino group of a guanidino group-containing compound such as arginine to give an arginine derivative shown by the formula (R is H or α-amino group- protecting group), which can be used for peptide synthesis. n PREPARATION: For example, 2,3,5-trimethyanisole is reacted with chlorosulfonic acid to give 4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride shown by the above example as crystal without forming an isomer. n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1988-11-10^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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