Big Chemical Encyclopedia

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

Articles Figures Tables About

Thymol methyl ether

This worker also found (Compt. rend. 150, 1061-3) by the fractionation of 1 kilo of the oil, /-limonene, cymene, thymol methyl ether and rf-pinene could be separated. [Pg.97]

Delepine Bull. Soc. Chem. 1918, 23 (iv), 24-35) states that the plant growing in different parts of France consistently contains the following characteristic substances dill-apiole, thymol methyl ether and crithmene. In some cases c/-pinene and a paraffin are also present. [Pg.97]

Thymol methyl ether, in 1-10048 Thymosin al (human), see T-30098 Thymosin al (ox), see T-30098 Thymus nucleic acid, see D-10041 Tienef, in T-30270 6a-Tigloyloxychaparrin, in H-10095 6y9-Tigloyloxyeuryopsin, in F-10033 13a-Tigloyloxymultiflorine, in M-10092 Tilifolidione, T-20123 Tinctomorone, in D-10180... [Pg.504]

Corsican Limbarda crithmoides L. ssp. longifolia (Asteraceae) essential oil was investigated, and it was found to contain 65 constituents, among which the major compounds werep-cymene, a-pinene, thymol-methyl-ether, 2,5-dimethoxy-p-cymenene, 3-methoxy-j9-cymenene, and a-phellandrene. In DPPH and ABTS assays, this essential oil showed positive results. A moderate reducing power of ferric ion was measured with FRAP assay and was attributed to the essential oil (Andreani et al., 2013). [Pg.335]

Thymol methyl ether (459) was converted by fungi A. niger, Mucor ramannianus, Rhizopus arrhizus, and Trichothecium roseum to give 7-hydroxy- (460) and 9-hydroxythymol methyl ether (461) (Demirci et al., 2001) (Figure 19.79),... [Pg.796]

FIGURE 19.106 Metabolic pathways of (-)-carvone (93 ) by Aspergillus niger TBUYN-2 and Absidia glauca ATCC 22752. (Modi ed from Demirci, F. et al.. The biotransformation of thymol methyl ether by dif ferent fungi. Book of Abstracts of the XII Biotechnology Congr., p. 47, 2001.)... [Pg.817]

Demirci, F., N. Kirimer, B. Demirci, Y. Noma, and K.H.C. Baser, 2001. The biotransformation of thymol methyl ether by different fungi. XIIBiotechnology Congr., Book of abstracts, p. 47. [Pg.727]

Contains up to 1% (normally about 0.3%) of a viscous volatile oil, about half of which is composed of fatty acids, with palmitic, lino-leic, myristic, and linolenic acids predominant. Aromatic constituents present include terpenes, thymol, thymol methyl ether, 4-hydroxy-thymol dimethyl ether, and isobutyric... [Pg.42]

Obtained by saponification of 3 -acetoxy-4-methoxy-2-methyl-5-isopropylbenzo-phenone (SM) with sodium hydroxide in dilute ethanol at reflux for 30 min (73%). SM was prepared by Friedel-Crafts acylation of thymol methyl ether with m-acetoxybenzoyl chloride in the presence of aluminium chloride in carbon disulfide at 0 for 20 h (12%) [990]. [Pg.186]

Obtained by reaction of chloroacetyl chloride on 3-methyl-4-isopropylanisole (p-thymol methyl ether) with aluminium chloride in carbon disulfide [4663],... [Pg.1252]

Me ether [1076-56-8]. l-Isopropyl-2-methoxy-4-methylbenzene. 2-Isopropyl-5-methylanisole. Thymol methyl ether C HjP M 164.247... [Pg.633]

Thymol, see 1-00075 Thymolbenzein, T-00180 Thymol blue, T-00181 Thymol methyl ether, in 1-00075 Thymolphthalein, T-00182 Thymolphthalein complexon, see T-00183 Thymolphthalexon, T-00183 Thymolphthalexon S, see M-00327 Thymolsulfonephthalein, see T-00181 Thymoltetrachlorophthalein, T-00184 Thyreosedine, see D-00341... [Pg.1058]


See other pages where Thymol methyl ether is mentioned: [Pg.674]    [Pg.674]    [Pg.288]    [Pg.674]    [Pg.1328]    [Pg.1328]    [Pg.67]    [Pg.674]    [Pg.674]    [Pg.526]    [Pg.334]    [Pg.748]    [Pg.796]    [Pg.797]    [Pg.895]    [Pg.586]    [Pg.631]    [Pg.632]    [Pg.726]    [Pg.186]    [Pg.2897]   
See also in sourсe #XX -- [ Pg.256 ]

See also in sourсe #XX -- [ Pg.631 ]

See also in sourсe #XX -- [ Pg.42 ]




SEARCH



Thymol

© 2024 chempedia.info