200:
24:
513:
Santos, Paula M.; Figueiredo, A. Cristina; Oliveira, M. Margarida; Barroso, José; Pedro, Luis G.; Deans, Stanley G.; Younus, A.K.M.; Scheffer, Johannes J.C. (1998). "Essential oils from hairy root cultures and from fruits and roots of
Pimpinella anisum".
239:
609:
786:
497:
214:
569:
541:
Martin, R.; Reichling, J.; Becker, H. (1985). "Reinvestigation of the
Phenylpropanoids from the Roots of Pimpinella Species".
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157:
602:
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331:
776:
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412:
377:
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195:
36:
715:
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67:
570:"Further Studies on the Biosynthesis of Pseudoisoeugenols in Tissue Cultures of Pimpinella anisum"
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730:
645:
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121:
781:
550:
523:
388:
262:
166:
77:
199:
376:. In addition to its standard form, the compound also occurs in a variety of structural
725:
325:
527:
770:
627:
619:
392:
367:
347:
313:
146:
400:
487:
740:
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23:
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112:
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445:
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Reichling, Jürgen; Galati, Enza Maria (2004). Jodral, Manuel Miró (ed.).
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133:
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Except where otherwise noted, data are given for materials in their
223:
InChI=1S/C10H12O2/c1-3-4-8-7-9(12-2)5-6-10(8)11/h3-7,11H,1-2H3/b4-3+
415:
100:
90:
574:
591:
444:
Biosynthesis of the compound is hypothesized to proceed via a
183:
492:(1st ed.). New York: CRC Press LLC. pp. 79–90.
395:
being associated with one of many possible esters in the
626:
380:. Common derivatives include the compound with its
145:
76:
603:
8:
318:357.3 °C (675.1 °F; 630.5 K)
481:
479:
477:
610:
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588:
568:Reichling, Jürgen; Martin, Rainer (1990).
198:
120:
15:
366:Pseudoisoeugenol naturally occurs in the
165:
473:
244:
219:
194:
370:of roots from plants within the genus
226:Key: CNTCZYAGRDSWBW-ONEGZZNKSA-N
7:
489:Illicium, Pimpinella and Foeniculum
136:
362:Natural occurrence and derivatives
14:
274:
22:
328:(at 25 °C , 100 kPa).
280:
268:
50:2-(1-Propenyl)-4-methoxyphenol
1:
528:10.1016/S0031-9422(98)00022-3
787:O-methylated natural phenols
432:, forms 2-methyl-5-methoxy
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346:is a naturally occurring
322:
255:
235:
210:
60:
47:
35:
30:
21:
422:of these esters, either
399:. Common esters include
413:2-methylpropionic acid
247:CC=CC1=C(C=CC(=C1)OC)O
555:10.1055/s-2007-969455
405:2-methylbutanoic acid
37:Preferred IUPAC name
298: g·mol
18:
332:Infobox references
41:4-Methoxy-2-phenol
16:
764:
763:
731:Methyl isoeugenol
340:Chemical compound
338:
337:
179:CompTox Dashboard
102:Interactive image
55:-Pseudoisoeugenol
17:Pseudoisoeugenol
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751:Pseudoisoeugenol
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580:(9–10): 942–948.
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389:functional group
344:Pseudoisoeugenol
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263:Chemical formula
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777:Phenylpropenes
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549:(3): 198–202.
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522:(3): 455–460.
516:Phytochemistry
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716:Isomyristicin
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706:Isodillapiole
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348:phenylpropene
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440:Biosynthesis
430:strong acids
428:or by using
423:
401:angelic acid
397:2nd position
371:
365:
343:
342:
61:Identifiers
52:
48:Other names
746:Osmorhizole
741:Nothoapiole
409:tiglic acid
384:bearing an
378:derivatives
256:Properties
771:Categories
736:Myristicin
721:Isosafrole
711:Isoeugenol
696:Exalatacin
676:Dillapiole
661:Chavibetol
468:References
462:Isoeugenol
434:benzofuran
420:Hydrolysis
382:side chain
373:Pimpinella
291:Molar mass
167:TQ75A9G9UX
113:ChemSpider
89:3D model (
78:98755-22-7
68:CAS Number
701:Isoapiole
686:Estragole
671:Croweacin
618:Types of
446:NIH shift
308:1.0 g/cm
681:Elemicin
666:Chavicol
656:Carpacin
646:Asaricin
636:Anethole
456:See also
450:anethole
391:and the
147:16116489
122:17273716
782:Phenols
756:Safrole
691:Eugenol
651:Asarone
425:in-vivo
386:epoxide
356:eugenol
350:and an
304:Density
296:164.204
134:PubChem
641:Apiole
496:
416:esters
411:, and
352:isomer
240:SMILES
31:Names
215:InChI
91:JSmol
53:trans
494:ISBN
158:UNII
551:doi
524:doi
448:of
354:of
184:EPA
137:CID
773::
578:45
576:.
572:.
547:51
545:.
520:48
518:.
476:^
452:.
436:.
418:.
407:,
403:,
358:.
278:12
272:10
611:e
604:t
597:v
557:.
553::
530:.
526::
502:.
284:2
281:O
275:H
269:C
186:)
182:(
93:)
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