http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S60228488-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_313f69d47526fdea2a26937b1eabf40b
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D519-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09J167-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-08
filingDate 1984-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ed01e22878054877c613ee34fdb8de8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e8078f67f09f423596e0426f10ff7a9
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b825602996c36d6eeac77aae38c6645
publicationDate 1985-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S60228488-A
titleOfInvention Bicycloorthoester compound
abstract NEW MATERIAL:A compound of formula I (R 1 and R 2 are alkyl). n EXAMPLE: The compound of formula II. n USE: A crosslinking agent, comonomer, etc. capable of giving a copolymer suitable for metal adhesives by reaction with a polyfunctional organic acid compound. n PREPARATION: For example, an orthoester compound of formula II (R 5 is alkyl; R 6 WR 6 " are alkyl), e.g. an orthopropionic acid triester, is reacted with dipentaerythritol of formula III in the presence of a catalyst, e.g. sulfobutyric acid, in an inert solvent, e.g. an aromatic hydrocarbon, at 80W250°C while removing an alcohol which is a reaction by-product by evaporation. n COPYRIGHT: (C)1985,JPO&Japio
priorityDate 1984-04-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 25.