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Merck

448575

Sigma-Aldrich

(−)-Guaiol

97%

Sinónimos:

(3R,6S,10S)-6,10,α,α-Tetramethylbicyclo[5.3.0]dec-1(7)-ene-3-methanol

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About This Item

Fórmula empírica (notación de Hill):
C15H26O
Número de CAS:
Peso molecular:
222.37
Beilstein/REAXYS Number:
2047993
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:

assay

97%

form

solid

optical activity

[α]20/D −28°, c = 4 in ethanol

mp

91-93 °C (lit.)

storage temp.

2-8°C

SMILES string

C[C@H]1CC[C@H](CC2=C1CC[C@@H]2C)C(C)(C)O

InChI

1S/C15H26O/c1-10-5-7-12(15(3,4)16)9-14-11(2)6-8-13(10)14/h10-12,16H,5-9H2,1-4H3/t10-,11-,12+/m0/s1

InChI key

TWVJWDMOZJXUID-SDDRHHMPSA-N

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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificados de análisis (COA)

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Muhammad Iqbal Choudhary et al.
Journal of natural products, 70(5), 849-852 (2007-03-28)
Microbial transformation of the sesquiterpene (-)-guaiol (1) [1(5)-guaien-11-ol] was investigated using three fungi, Rhizopus stolonifer, Cunninghamella elegans, and Macrophomina phaseolina. Fungal transformation of 1 with Rhizopus stolonifer yielded a hydroxylated product, 1-guaiene-9 beta,11-diol (2). In turn, Cunninghamella elegans afforded two
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Cancer biology & therapy, 19(8), 706-714 (2018-04-04)
(-)-Guaiol, a sesquiterpene alcohol with the guaiane skeleton, has been found in many Chinese medicinal plants and been reported to comprise various guaiane natural products that are well known for their antibacterial activities. Previously, we have shown its antitumor activity
Emma-Tuulia Tolonen et al.
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Thermal decomposition of dolomite in the presence of CO2 in a calcination environment is investigated by means of in situ X-ray diffraction (XRD) and thermogravimetric analysis (TGA). The in situ XRD results suggest that dolomite decomposes directly at a temperature

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