Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

7-Octen

For molecules similar to safrole or allylbenzene we take the work done on any terminal alkene such as 1-heptene, 1 octene. Another term to look for is olefin which is a term for a doublebond containing species. What we then look for are articles about these olefins where the functional groups we are looking for are formed. Articles with terminology like methyl ketones from (P2P), ketones from , amines from etc. Or when we want to see about new ways to aminate a ketone (make final product from P2P) we look for any article about ketones where amines are formed. Sound like science fiction to you Well, how do you think we came up with half the recipes in this book It works ... [Pg.183]

Tnmethyl 1 butene gives only (CH3)3CC=CH2 1 Octene gives a mixture of... [Pg.1216]

Content of Ot-Olefin. An increase in the a-olefin content of a copolymer results in a decrease of both crystallinity and density, accompanied by a significant reduction of the polymer mechanical modulus (stiffness). Eor example, the modulus values of ethylene—1-butene copolymers with a nonuniform compositional distribution decrease as shown in Table 2 (6). A similar dependence exists for ethylene—1-octene copolymers with uniform branching distribution (7), even though all such materials are, in general, much more elastic (see Table 2). An increase in the a-olefin content in the copolymers also results in a decrease of their tensile strength but a small increase in the elongation at break (8). These two dependencies, however, are not as pronounced as that for the resin modulus. [Pg.396]

Property Copolymer of ethylene and 1-butene Copolymer of ethy and 1-octene... [Pg.396]

Other Higher Oleiins. Linear a-olefins, such as 1-hexene and 1-octene, are produced by catalytic oligomerization of ethylene with triethyl aluminum (6) or with nickel-based catalysts (7—9) (see Olefins, higher). Olefins with branched alkyl groups are usually produced by catalytic dehydration of corresponding alcohols. For example, 3-methyl-1-butene is produced from isoamyl alcohol using base-treated alumina (15). [Pg.425]


See other pages where 7-Octen is mentioned: [Pg.436]    [Pg.437]    [Pg.438]    [Pg.439]    [Pg.242]    [Pg.76]    [Pg.76]    [Pg.77]    [Pg.185]    [Pg.23]    [Pg.263]    [Pg.396]    [Pg.398]    [Pg.514]    [Pg.618]    [Pg.642]    [Pg.642]    [Pg.1193]    [Pg.292]    [Pg.411]    [Pg.460]    [Pg.483]    [Pg.504]    [Pg.524]    [Pg.527]    [Pg.570]    [Pg.605]    [Pg.685]    [Pg.697]    [Pg.697]    [Pg.697]    [Pg.517]    [Pg.394]    [Pg.394]    [Pg.396]    [Pg.396]    [Pg.396]    [Pg.397]    [Pg.400]    [Pg.401]    [Pg.402]    [Pg.403]    [Pg.404]    [Pg.404]    [Pg.426]    [Pg.428]   
See also in sourсe #XX -- [ Pg.3 , Pg.76 ]

See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.3 ]




SEARCH



1 - Hydroxy-3,7-dimethyl-6-octen

1 -Fluoro-1 -octene, preparation

1 -Octen-3 -hydroperoxide

1- Methylbicyclo octenes

1- Octen synthesis

1- Octen-3-yl Butyrate

1- Octene infrared spectrum

1- Octene, reaction with ruthenium

1- Octene, reaction with ruthenium complexes

1-Octene

1-Octene

1-Octene Lewis acid catalysis

1-Octene catalysts, rhodium complexes

1-Octene ene reactions

1-Octene hydrosilylation

1-Octene metathesis

1-Octene ozonide

1-Octene, hydration

1-Octene, hydrosilylation with

1-Octene, oxidation

1-Octene, photochemical oxidation

1-octene liberation

1-octene liberation from

1-octene selectivity

1-octene, copolymerisation

1.2- Epoxy-7-octene

1.5- Diazabicyclo octenes

2- -l-octene

2- Methyl-4-octene

2-Methyl-6-methylen-7-octen

2-Methyl-6-methylene-7-octen

2-Methyl-l-octene

2-Methylbicyclo octene

2-butyl-2-octenal

2.6- Dimethyi-7-octen

2.6- Dimethyl-7-octene-2,3,6-triol

3,7-Dimethyl-l-octene

3- Octanol 2-Octen

3- Octen-2-one

3- methyl-4-propyl-3-octene

3-Octen-l-one

3-Oxabicyclo -7-octene-6-ones

3.7- Dimethyl-3-phenyl-7-octene

3.7- Dimethyl-6-octen

3.7- Dimethyl-6-octen-l-yl Acetate

3.7- Dimethyl-6-octene

4- Octene oxide

4-Ethyl-2-octene

4-Hydroxy-2,3-octenal

4-Octene-l,8-diol

4-chloro-4-octene, oxidation

5-methylenebicyclo octene

5.6- Dioxabicyclo octene

6- Ethyl-3-methyl-3-octene

6- Octenal, 3,7-dimethyl

6-Octen-3-one, 8-bromo-4-methylcyclization

6-Octen-3-one, 8-bromo-4-methylcyclization samarium diiodide

6-Octen-l-yne

6-Octen-l-yne intramolecular ene reaction

6-Octenal, 7-methylene reaction

8-Bromo-1-octene

A-octene

Analysis of l-Octen-3-one

Aroma octen

Asymmetric 1 -octene

Benzobicyclo octene

Benzobicyclo octene system

Bicyclo 3.3.0]octenes

Bicyclo octene

Bicyclo octene annelated with

Bicyclo octene cations

Bicyclo octene conjugation

Bicyclo octene frameworks

Bicyclo octene molecular structures of radical

Bicyclo octene oligothiophenes

Bicyclo octene oxidation

Bicyclo octene ring

Bicyclo octene synthesis

Bicyclo octene via cyclization of alkynes

Bicyclo octene, vinylCope rearrangement

Bicyclo octene-7,8-diones

Bicyclo octenes synthesis

Bicyclo[2.2.2 octene derivative

Bicydo 3.3.0 octenes

C/s-2-octene

Carbon octene

Charge 1-octene

Chloroform, reaction with 1-octene

Cis-2-Octene

Crystallinity ethylene-octene copolymer

CsHi« 1-Octene

Cw-3-Octen

Cyclization reaction of 6-octen

Cyclo-octene

Cyclo-octene 1-phenyl

Cydo-octene

ETHYLENE-OCTENE

ETHYLENE-OCTENE COPOLYMER

Elastomeric ethylene-octene copolymer

Enzymes 2-Octenal

Epoxidation 1-octene

Ethene-1-octene

Ethylene octene, metallocene-type

Ethylene-1-octene copolymer density

Ethylene-l-octene copolymer

Ethylene-octene copolymer curves

Ethylene-octene copolymer elastomers

Ethylene-octene copolymer, Engage

Ethylene-octene copolymers peak melting temperatures

F 1-Octene

Fragmentation bicyclo octene ring

Frans-2-Octenal

Frans-4-Octene

Homogeneous Copolymers of Ethylene-1-Octene

Hydroformylation 1-octene

Hydroformylation of 1-octene

Hydroformylation trans-4-octene

Hydroformylations of 1-octene

Hydrogen acceptor, 1-octene

Hydrogenation 1-octene

Hydrogenation of 1-octene

Hydrosilylation of 1-octene

I- Octen

I-Octene

Isomeric 2-octenes

Isomerization 2-octene

Isomerization n-octene mixtures

Kinetics 1-octene

L-Octen

L-Octen-3-yl Acetate

L-Octen-3-yl Butyrate

L-Octene-4-yne

Linear ethylene/octene copolymer

Lithium, l-octen-2-ylsynthesis

Mixed 2-Octenes

N-octene

OCTENE COPOLYMER

Octen mushroom aroma

Octen-3-ol

Octenal

Octenal

Octenal, -2-, linoleic acid, autoxidation

Octene comonomer

Octene hydrozirconation

Octene isomerization, base catalyzed

Octene isomers

Octene optimized conditions

Octene silane conversion

Octene terminal alkynes catalyzed

Octene, from octyne

Octene-propylene copolymer

Octenes

Octenes

Octenes 1-octene

Octenes 1-octene

Octenes epoxidation

Octenes hydroformylation

Octenes isomerisation

Octenes isomerizations

Octenes metathesis

Octenes, addition

Octenes, cracking

Octenes, reaction

Oxabicyclo octene

Oxabicyclo octenes

Palladium 1-octene

Phosphabicyclo octene

Phosphabicyclo octene 2-oxides

Phosphabicyclo octenes

Polymer 1-octene, hydroformylation

Process Design for Hydroformylating Octenes at the University of Kansas

Process Synthesis for the Fluorous Biphasic Hydroformylation of 1-Octene

Regioselective isomeric 2-octenes

Regioselective trans-2-octene

Rrans-2-Octenal

Ruthenium catalyzed 2-octene

Selective 1 -octene

Tetracyclo octene

Trans-2-OCTENE.53(Vol

Trans-2-Octenal

Trans-3-Octene

Trans-4-octene, isomerization/hydroformylation

Tricyclo 3.3.1.0]octenes

© 2024 chempedia.info