http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9108940-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e1724b6a956b9ec32aa3aa9112e7fb0b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d2388d1956e61bb526f14c686b73810b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a289c3d1441ccb144e571512ef44b437
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-68
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-68
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-02
filingDate 2014-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_115f856e019c179b4ec451f6f32fc947
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9cdd5a92d957bf85f05ff634d13b871b
publicationDate 2015-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9108940-B2
titleOfInvention Conversion of 5-(chloromethyl)-2-furaldehyde into 5-methyl-2-furoic acid and derivatives thereof
abstract The present invention concerns the synthesis of 5-methyl-2-furoic acid, including ester, amide, and thioester derivatives of such from 5-(chloromethyl)-2-furaldehyde (CMF). The molecules so prepared are useful as intermediates for pharmaceutical, food, and fragrance molecules; as well as fuel or fuel additives.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9783517-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2015203462-A1
priorityDate 2010-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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