(+)-Ledene

(+)-Ledene
Compound Structure:
Synonyms: (+)-Ledene;Viridiflorene;Ledene;21747-46-6;Leden;(1aR,7R,7aS,7bR)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydro-1H-cyclopropa[e]azulene;236ZZ41F70;1H-Cycloprop(e)azulene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,4,7-tetramethyl-, (+)-;EINECS 244-565-3;MFCD0004
Compound ID: NMPC-017
PubChem ID:

10910653

Molecular Formula: C15H24
Canonical SMILES: CC1CCC2=C(CCC3C(C12)C3(C)C)C
InChIKey: WGTRJVCFDUCKCM-FMKGYKFTSA-N
About the compound:

(+)-Ledene, also recognized as (+)-viridiflorene, is a distinct compound in the field of chemistry, categorized as a sesquiterpene. This compound is identifiable by its molecular formula, C15H24, and is noted for its tricyclic sesquiterpene structure. The prefix "(+)" in its name signifies its status as a positive enantiomer, which is characterized by its ability to rotate plane-polarized light in a clockwise direction. In the realm of natural sciences, (+)-Ledene is found in a variety of plant species. It is particularly prominent in certain essential oils derived from the Labiatae family, showcasing its natural prevalence. The applications of (+)-Ledene are diverse and significant. In the fragrance industry, its aromatic qualities make it a valuable component for perfumes, contributing to the creation of appealing scents. Beyond its olfactory benefits, (+)-Ledene is also a subject of scientific curiosity in research. Its potential biological activities make it an interesting candidate for various studies. Moreover, in the field of organic synthesis, it serves as a precursor, highlighting its versatility and importance in chemical research and applications.

Properties:

Chemical and Physical Properties

Property Name

Property Value

Molecular Weight

204.35 g/mol

XLogP3-AA

4

Hydrogen Bond Donor Count

0

Hydrogen Bond Acceptor Count

0

Rotatable Bond Count

0

Exact Mass

204.187800766 g/mol

Monoisotopic Mass

204.187800766 g/mol

Topological Polar Surface Area

0²

Heavy Atom Count

15

Formal Charge

0

Complexity

321

Isotope Atom Count

0

Defined Atom Stereocenter Count

4

Undefined Atom Stereocenter Count

0

Defined Bond Stereocenter Count

0

Undefined Bond Stereocenter Count

0

Covalently-Bonded Unit Count

1

Compound Is Canonicalized

Yes

Source: PubChem

Source Species: Hirsute Palisota
Eucalyptus cloeziana
Eugenia uniflora
Murraya Koenigii
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