SpectraBase Compound ID | HN9e5Q3eR9l |
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InChI | InChI=1S/C16H28O/c1-14(2)8-5-9-15(3)12(14)6-10-16(4)13(15)7-11-17-16/h12-13H,5-11H2,1-4H3/t12-,13+,15-,16+/m0/s1 |
InChIKey | YPZUZOLGGMJZJO-LQKXBSAESA-N |
Mol Weight | 236.4 g/mol |
Molecular Formula | C16H28O |
Exact Mass | 236.214016 g/mol |
Enantiomer InChIKey | YPZUZOLGGMJZJO-CLWVCHIJSA-N |
Copyright | Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved. |
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Source of Spectrum | Adams' Essential Oil Components (GC-MS), Version 4 |
Copyright | Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved. |
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Source of Spectrum | Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy) |
Title | Journal or Book | Year |
---|---|---|
Chiral Decalins: Preparation from Oleanolic Acid and Application in the Synthesis of (−)-9-epi-Ambrox | Journal of Natural Products | 2006 |
Synthesis of d,l-Norlabdane Oxide and Related Odorants: An Intramolecular Radical Approach | The Journal of Organic Chemistry | 1998 |
The biotransformation of Ambrox® and sclareolide by Cephalosporium aphidicola | Phytochemistry | 1996 |
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