http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-238253-B1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_04178b4559d39eedd00af01bd8a6beee
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6c04e68556d18a05e3a2969820b97be2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1970dc1dde2ae2ae442b5c0aedc63ccc
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B35-18
filingDate 1983-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8867dad155551da9ac5c4dd98223e194
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_33836666c7be37f20112b14b8bb0f557
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b121ad20fabc93310639aefa2c85508b
publicationDate 1985-11-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CS-238253-B1
titleOfInvention Process for the production of 1-dimethylamine-1-carba-clododecaborane (II)
abstract The invention relates to the field of boron chemistry andnsolves a simple process for the production of 1-dimethylamine-1-carboxylic acid dodecaboranen(11)nΙ-ζΟΗ ^ οΝΗ-Ι-ΟΒιiHip. This compound doesnprepared by heating 7-trimethylamine-7-carbanido-undecarborane (12)nwith triethylaminborane (3)nat 150 to 210 ° C for 8 ton50 hours * and the reaction mixture is then subjected tonmethanolysis in an acid medium, withna pure product in a yield of over 80% is obtainednacidifying the aqueous alkaline leachatenproduct of methanolysis. Said compoundnis used as a preparation for neutronncapture tumors and for modificationnbiologically active organic compounds.
priorityDate 1983-05-27-04:00^^<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: 24.