74327
Sclareol
purum, ≥95.0% (GC)
Synonym(s):
(1R,2R,8aS)-Decahydro-1-(3-hydroxy-3-methyl-4-pentenyl)-2,5,5,8a-tetramethyl-2-naphthol
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About This Item
Empirical Formula (Hill Notation):
C20H36O2
CAS Number:
Molecular Weight:
308.50
EC Number:
208-194-0
UNSPSC Code:
12352000
MDL number:
Beilstein/REAXYS Number:
2054148
grade
purum
assay
≥95.0% (GC)
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
218-220 °C/19 mmHg (lit.)
mp
95-100 °C (lit.), 98-103 °C
SMILES string
CC1(C)CCC[C@@]2(C)[C@H]1CC[C@@](C)(O)[C@@H]2CC[C@@](C)(O)C=C
InChI
1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18-,19-,20+/m0/s1
InChI key
XVULBTBTFGYVRC-HHUCQEJWSA-N
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Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Jean-Claude Caissard et al.
PloS one, 7(10), e48253-e48253 (2012-11-08)
Sclareol is a high-value natural product obtained by solid/liquid extraction of clary sage (Salvia sclarea L.) inflorescences. Because processes of excretion and accumulation of this labdane diterpene are unknown, the aim of this work was to gain knowledge on its
Ariana B Souza et al.
Molecules (Basel, Switzerland), 16(11), 9611-9619 (2011-11-22)
The antimicrobial activity of four labdane-type diterpenes isolated from the oleoresin of Copaifera langsdorffii as well as of two commercially available diterpenes (sclareol and manool) was investigated against a representative panel of microorganisms responsible for periodontitis. Among all the evaluated
E J Alvarez-Manzaneda et al.
Organic letters, 7(8), 1477-1480 (2005-04-09)
[reaction: see text] A new route toward puupehenone-related bioactive metabolites from (-)-sclareol, based on the palladium(II)-mediated diastereoselective cyclization of a drimenylphenol, is described. Utilizing this, the first enantiospecific synthesis of the antitumor and antimalarial (-)-15-oxopuupehenol, together with improved syntheses of