5,10-cycloaromadendrane sesquiterpenoids

Description:

Aromadendrane sesquiterpenoids that arise from the C5-C10 cyclization of the aromadendrane skeleton.

Ancestors:

Organic compounds ⮕ Lipids and lipid-like molecules ⮕ Prenol lipids ⮕ Sesquiterpenoids ⮕ Aromadendrane sesquiterpenoids ⮕ 5,10-cycloaromadendrane sesquiterpenoids

Spathulenol
- ≥95%
Cas Number: 6750-60-3 Compound CID: 92231

IUPAC Name: (1aR,4aR,7S,7aR,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol

SMILES: CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C

InChIKey: FRMCCTDTYSRUBE-BGPZULBFSA-N

InChI: InChI=1S/C15H24O/c1-9-5-6-11-13(14(11,2)3)12-10(9)7-8-15(12,4)16/h10-13,16H,1,5-8H2,2-4H3/t10-,11+,12+,13+,15-/m0/s1
Details

Pricing Close
(−)-Globulol
- ≥98.5%(GC)
- sum of enantiomers
Cas Number: 489-41-8 Compound CID: 12304985

Formula: C₁₅H₂₆O Molecular Weight: 222.37

IUPAC Name: (1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol

SMILES: C[C@@H]1CC[C@@H]2[C@@H]1[C@H]3[C@@H](CC[C@@]2(C)O)C3(C)C

InChIKey: AYXPYQRXGNDJFU-QTPLKFIXSA-N

InChI: InChI=1S/C15H26O/c1-9-5-6-10-12(9)13-11(14(13,2)3)7-8-15(10,4)16/h9-13,16H,5-8H2,1-4H3/t9-,10-,11-,12-,13-,15-/m1/s1

Synonyms: Globulol | (1aR,4R,4aR,7R,7aS,7bS)-Decahydro-1,1,4,7-tetramethyl-1H-cycloprop[e]azulen-4-ol
Details

Pricing Close
(+)-Ledene
- ≥95%(GC)(sum of enantiomers)
Cas Number: 21747-46-6

Formula: C₁₅H₂₄ Molecular Weight: 204.35

IUPAC Name: (1aR,7R,7aS,7bR)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene

SMILES: CC1CCC2=C(CCC3C(C12)C3(C)C)C

InChIKey: WGTRJVCFDUCKCM-FMKGYKFTSA-N

InChI: InChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h10,12-14H,5-8H2,1-4H3/t10-,12-,13-,14-/m1/s1

Synonyms: C20162 | CHEBI:63444 | (+)-Ledene, >=95.0% (sum of enantiomers, GC) | 1,1,4,7-tetramethyl-1alpha,2,3,5,6,7,7alpha,7b-...
Details

Pricing Close

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