Global Information Lookup Global Information

Perillene information


Perillene
Names
Preferred IUPAC name
3-(4-Methylpent-3-en-1-yl)furan
Other names
Perillen; 3-Homoprenylfuran
Identifiers
CAS Number
  • 539-52-6 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:74039
ChemSpider
  • 61612
PubChem CID
  • 68316
UNII
  • AM4D4646ZW checkY
CompTox Dashboard (EPA)
  • DTXSID40202167 Edit this at Wikidata
InChI
  • InChI=1S/C10H14O/c1-9(2)4-3-5-10-6-7-11-8-10/h4,6-8H,3,5H2,1-2H3
    Key: XNGKCOFXDHYSGR-UHFFFAOYSA-N
SMILES
  • o1ccc(c1)CC\C=C(/C)C
Properties
Chemical formula
C10H14O
Molar mass 150.221 g·mol−1
Appearance liquid
Density 0.9017 g/mL @ 20 °C
Boiling point 186 °C (367 °F; 459 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Perillene is a natural monoterpene that consists of a furan ring with a six-carbon homoprenyl side chain. Perillene is a component of the essential oil obtained by extraction of the leaves of Perilla frutescens.[1] Perillene has also been obtained by steam distillation of the leaves of Perilla frutescens.[2] Perillene has been found to elicit distinct electrophysiological responses in the antennae of the apple blossom weevil. It has been suggested that perillene is one several molecules in the emanation bouquet of apple tree buds which may be used by adult weevils as chemical cues to discrimination during host-searching behavior.[3]

  1. ^ Jiawen Yu, “Fingerprint identification of Perilla oil containing perillaldehyde and perillene with anti-inflammatory, intestinal motility promoting and bactericidal effects”, CN Patent 101,669,992 (2010)
  2. ^ Yuling Qing, “New use of perillene for preparing anti-inflammatory pharmaceutical formulations”, CN Patent CN 101,874,797 A 20,101,103 (2010)
  3. ^ Blanka Kalinova; Stransky, Karel; Harmatha, Juraj; Ctvrtecka, Richard; Zd'arek, Jan (2000). "Can chemical cues from blossom buds influence cultivar preference in the apple blossom weevil (Anthonomus pomorum)?". Entomologia Experimentalis et Applicata. 95 (1): 47–52. doi:10.1046/j.1570-7458.2000.00640.x.

and 6 Related for: Perillene information

Request time (Page generated in 0.5173 seconds.)

Perillene

Last Update:

Perillene is a natural monoterpene that consists of a furan ring with a six-carbon homoprenyl side chain. Perillene is a component of the essential oil...

Word Count : 231

C10H14O

Last Update:

rosemary essential oil Levoverbenone Menthofuran Penguinone Perillaldehyde Perillene Rosefuran Safranal Thymol Umbellulone Verbenone This set index page lists...

Word Count : 83

Perilla ketone

Last Update:

3-furyl-organotin compound and isocaproyl chloride in tetrahydrofuran solvent. Perillene Sebe, Yeigai (1943). "Supplemental experiments on perilla ketone". Nippon...

Word Count : 243

Shiso

Last Update:

with an IC50 of 23.2 μM. Other chemotypes include eschscholzia ketone, perillene, and the phenylpropanoids myristicin, dillapiole, elemicin, citral, and...

Word Count : 4114

Rosefuran

Last Update:

Seiichi Takano; Morimoto, Masamichi; Satoh, Shigeki (1984). "Syntheses of perillene and rosefuran from common starting materials". Chemistry Letters. 7: 1261–1262...

Word Count : 753

Hippeastrum calyptratum

Last Update:

to burnt plastic is composed of the following compounds: 1,8-cineole, perillene, camphor, linalool, limonene, g-terpinene, b-myrcene, sabinene, a-pinene...

Word Count : 585

PDF Search Engine © AllGlobal.net