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Merck
CN

74327

香紫苏醇

purum, ≥95.0% (GC)

别名:

(1R,2R,8aS)-十氢-1-(3-羟基-3-甲基-4-戊烯基)-2,5,5,8a-四甲基-2-萘酚

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关于此项目

经验公式(希尔记法):
C20H36O2
化学文摘社编号:
分子量:
308.50
EC Number:
208-194-0
UNSPSC Code:
12352000
MDL number:
Beilstein/REAXYS Number:
2054148
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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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存储类别

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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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