Methyl 9-octadecenoate

Methyl-9-octadecenoate, metathesis of, 24 13 Methyl orange, polyethyleneimine binding, 29 216-217... 

Saturated fatty acids with alkyl branching like e.g. (R,S)-tuberculostearic acid 39 are formed by olefination of 36 with ketone 37, hydrogenation of the resulting methyl 10-methyl-9-octadecenoate 38 with Raney-nickel and subsequent hydrolysis 66). 

SYNS EMEREST2301 ExMEREST2801 EMERY 2219 EMERY 2310 EMERY OLEIC ACID ESTER 2301 KEMESTER 105 KEMESTER 115 0 KEMESTER 205 KEMESTER 213 METHYL-9-OCTADECENOATE METHYL ds-9-OCTADECENOATE METHYL (Z)-9-OCTADECENOATE METHYL OLEATE (Z)-9-OCTADECENOIC ACID METHYL ESTER... 

METHYL-n-NONYL KETONE see UKSOOO N-METHYLNOREPHEDRINE see EAWOOO METHYL OCTADECANOATE see MJWOOO METHYL-9-OCTADECENOATE see OHWOOO METHYL (Z)-9-OCTADECENOATE see OHWOOO METHYL cis-9-OCTADECENOATE see OHWOOO... 

Synonyms methyl 9-octadecenoate (Z)-9-octadecenoic acid, methyl ester. 

Methylnottane. See Isododecane 8-Methylnonanoic acid. See Isodecanoic acid Methyl cis,cis-9,12-octadecadienoate. See Methyl linoleate Methyl octadecanoate Methyl n-octadecanoate. See Methyl stearate Methyl 9-octadecenoate Methyl-cis-9-octadecetroate Methyl (Z)-9-octadecenoate. See Methyl oleate 7-Methyl-1-octanol 7-Methyloctyl alcohol. See Isononyl alcohol... 

CAS 112-62-9 67762-38-3 EINECS/ELINCS 203-992-5 267-015-4 Synonyms Methyl 9-octadecenoate Methyl-cis-9-octadecenoate Methyl (Z)-9-octadecenoate 9-Octadecenoic acid, methyl ester (Z)-9-Octadecenoic acid, methyl ester Oleic acid, methyl ester, cis- cis-Oleic acid, methyl ester... 

D-Glucopyranoside, methyl, octadecanoate (2 3). See Methyl glucose sesquistearate D-Glucopyranoside, methyl, 9-octadecenoate (2 3). See Methyl glucose sesquioleate a-D-Qlucopyranoside, 1,3,4,6-tetra-O-acetyl-p-D-fructofuranosyl-, tetraacetate. See Sucrose octaacetate... 

Synonyms Methyl 9-octadecenoate Methyl-cis-9-octadecenoate Methyl (Z)-9-octadecenoate 9-Octadecenoic acid, methyl ester (Z)-9-Octadecenoic acid, methyl ester... 

Apart from halogen substituted alkenes, heteroatoms normally deactivate catalytic systems. However the synthetic utility of such reactions has encouraged further research in this field. Chlorine substitution at vinylic positions deactivates the double bond but halogen substituted alkenes in which the double bond is in an position undergo cross metathesis with internal alkenes. For example, 5-bromo-l-pentene undergoes cross metathesis with 2-pentene. Unsaturated compounds containing ester groups also react, e.g. methyl-9-octadecenoate is converted to 9-octadiene and dimethyl-9-octadecenedioate by the WCl —Sn(CH3)4 catalytic combination [15]. 

Formulate a mechanism for the reaction of methyl 9-octadecenoate with 1-dodecanamine shown on p. 900. 

D-Glucopyranoside, methyl, 9-octadecenoate (2 3). See Methyl glucose sesqul-oleate... 

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