http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-401712-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_df95b7537b79b8acbdd481a7360f23df
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F3-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F3-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-22
filingDate 1972-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1975-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-401712-A1
titleOfInvention A METHOD TO PREPARE SUBSTANTIALLY PURE ASYMMETRIC TRIORGANOESTANE HALIDES WITH HIGH YIELDS.
abstract A method of preparing in high yields substantially pure asymmetric triorganotin halides of the formula RnR'(3-n) SnX, wherein R represents a linear aliphatic hydrocarbon monovalent radical containing up to six carbon atoms, R' represents a hydrocarbon monovalent radical aliphatic or cycloaliphatic containing up to eight carbon atoms, with the stipulation that the molecular weight of R'exceeds that of R by at least 42 grams per mole except when R' is a cycloaliphatic hydrocarbon radical, X represents an atom of chlorine or bromine, and n is an integer selected from 1 and 2, said method comprising; reacting substantially equimolar amounts of a tetraorganostannic compound R (n + l) R'(3-n) Sn and a stannic tetrahalide SnX4, adding a suitable solvent to dissolve the RSnX3 by-product, and isolating the triorganotin halide in substantially pure form. (Machine-translation by Google Translate, not legally binding)
priorityDate 1971-04-14-04:00^^<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: 19.