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2 -Pinen

Pinene hydrochloride is prepared in the usual manner from turpentine, and this is allowed to react with acetate of silver. Isobornyl acatate is formed, which is hydrolysed, and the isoborneol oxidised to camphor. Acetate of lead is also used, as is also acetate of zinc. [Pg.242]

Common Name a-Pinene Synonym dl-pinene, 2-pinene... [Pg.373]

Lemon peel oil is much more valuable than its juice therefore, extensive research efforts have been expended to determine its natural composition as a way to detect adulteration as well as to determine quality factors [6, 31, 32]. However, a few studies on lemon juice volatiles can be found [33-35]. Lemon oils are notable for possessing relatively low levels of limonene (more than 70%) and relatively high levels of a-pinene (1-2%), -pinene (6-13%), sabinene (1-2%) and y-terpinene (8-10%) [32]. The relatively high concentration of -pinene is thought to instil the green peely odour of lemon oil. The concentrations of aliphatic and monoterpenic aldehydes, (especially citral) as well as those of esters and alcohols are critical components in the perceived quality of the oil. As lemon oil is unstable, quality can deteriorate with improper storage, resulting in... [Pg.122]

For a double bond within the ring, only one prefix number is necessary — that of the lower-numbered carbon to which the double bond is attached — e.g., 3-thujene (Formula 48, Chart 10) 2-pinene (Formula 67, Chart 12). [Pg.41]


See other pages where 2 -Pinen is mentioned: [Pg.264]    [Pg.213]    [Pg.123]    [Pg.683]    [Pg.130]    [Pg.1100]    [Pg.35]    [Pg.184]    [Pg.17]    [Pg.16]    [Pg.51]    [Pg.257]    [Pg.36]    [Pg.263]    [Pg.1154]    [Pg.2151]    [Pg.2221]    [Pg.6]    [Pg.49]    [Pg.49]    [Pg.86]    [Pg.87]    [Pg.97]    [Pg.98]    [Pg.1100]    [Pg.157]    [Pg.65]    [Pg.270]    [Pg.229]    [Pg.614]    [Pg.86]    [Pg.115]   
See also in sourсe #XX -- [ Pg.3 , Pg.17 , Pg.53 ]

See also in sourсe #XX -- [ Pg.3 , Pg.17 , Pg.53 ]




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0-Pinene photooxidation

0-Pinene transitions

0-Pinene, hydrosilylation

2-Pinene

2-Pinene

3- Indolyl-acetonitrile with -P-pinene

3-Pinene reduction

8-Pinene synthesis

8-Pinene via methyllithium addition

A, P -pinene

A-Pinene Ritter reaction

A-Pinene diimide

A-Pinene epoxide

A-Pinene hydroboration

A-Pinene hydroformylation

A-Pinene hydrosilylation

A-Pinene metallation

A-Pinene oxidation

A-Pinene oxide

A-Pinene oxide, preparation

A-Pinene photooxidation

A-Pinene rearrangement

A-Pinene turpentine

A-Pinene,

A-Pinene, 7-trimethylsilylacylation

A-Pinene, 7-trimethylsilylacylation Friedel-Crafts reaction

A-Pinene, 7-trimethylsilylacylation allylboranes from

A-Pinene, 7-trimethylsilylacylation reactions with aldehydes

A-Pinene, ozonolysis

A-Pinenes

Allylboranes pinene-derived

Alpha pinene, structure

Alpha-PINENE.200(Vol

Alpha-pinene

Atmosphere pinene reactions

B-pinene

Beta-PINENE.201(Vol

Beta-pinene

Camphene, from pinene

Camphor from a-pinene

Central from pinenes

Chromatographic separations example, pinenes separation

Copolymerizations using pinenes

Ct-Pinene

D-a-pinene

D-pinene

Degradation of a-pinene

Diastereoselective hydroformylation 3-pinene

Enantiomeric composition of a-pinene

Fi-Pinene

G-Pinene

HERCULES alpha-Pinene

Hydration, of a-pinene

Hypericum perforatum a-pinene from

Isomerization of -P-pinene

Isomerization of -a-pinene

Isomerization of a-pinene oxide

J8-Pinene

JS-Pinene

Kinetics of a-Pinene Isomerization

Living cationic pinene

Monoterpenes metabolism pinene

Myrcene synthesis from 0-pinene

N-Pinene

O-Pinene

Ot-pinene

Other Reactions of Pinene

Oxidation pinenes

Ozone, atmosphere pinene reactions

Ozonolysis 3-pinene

Ozonolysis of a-pinene

Ozonolysis pinenes

P-Pinene

PINENE, BICYCL0 HEPT-2-ENE

PINENE, HEPTANE, 6.6-DIMETHYL-2-METHYLENE

PMR Analysis of Poly(isobutylene-co-3-Pinene)

Physical chemistry 3-pinene

Pinacol rearrangement pinene

Pinane, Pinene

Pinene Cinnamon

Pinene Nitrosochloride

Pinene a- and

Pinene and Derivatives for Stereospecific Syntheses of Chiral Monoterpenes

Pinene cyclase

Pinene derivative

Pinene hydrochloride

Pinene hydroperoxide

Pinene isomerization

Pinene orange

Pinene oxidation

Pinene oxide

Pinene oxides, rearrangement

Pinene pepper

Pinene protonation

Pinene pyrolysis

Pinene synthase

Pinene synthases

Pinene, Wagner-Meerwein rearrangement with

Pinene, aCH COLOC

Pinene, adsorption

Pinene, atmosphere

Pinene, racemization

Pinenes

Pinenes alpha

Pinenes aroma

Pinenes borneol from

Pinenes citral from

Pinenes dipentene and

Pinenes fenchone from

Pinenes fragmentation

Pinenes from Turpentine

Pinenes molecular structure

Pinenes odor type

Pinenes pyrolysis

Pinenes separation, chromatographic

Pinenes terpene derivatives from

Pinenes, rearrangement

Planar from pinenes

Racemization of pinene

S-Pinene

Separation of Pinenes

Troposphere pinene reactions

Turpentine 0(-pinene

Z-a-Pinene

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