Introduction:Basic information about CAS 2524-37-0|Ethyl orsellinate, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Ethyl orsellinate is a lichen metabolite and a derivative of lecanoric acid with antiproliferative and antitumour activities[1]. Ethyl Orsellinate is against A. salina for the cytotoxic activity with an LC50 of 495 μM[2].
Related Catalog
Research Areas >>CancerResearch Areas >>InfectionSignaling Pathways >>Anti-infection >>Bacterial
In Vitro
Ethyl Orsellinate (0-50 μg/ml; 48 hours) inhibits Hep-2 cells, MCF-7 breast cancer cells, and 786-0 kidney carcinoma cells, as well as B16-F10 murine melanoma and non-cancerous Vero cells (IC50s=31.2, 70.3, 47.5, 64.8, and 28.1 µg/ml, respectively)[2].
References
[1]. Bogo D, et al. In vitro antitumour activity of orsellinates. Z Naturforsch C. 2010 Jan-Feb;65(1-2):43-8.
[2]. Gomes AT, et al. Cytotoxic activity of orsellinates. Z Naturforsch C. 2006 Sep-Oct;61(9-10):653-7.
Chemical & Physical Properties
Density
1.3±0.1 g/cm3
Boiling Point
349.5±22.0 °C at 760 mmHg
Melting Point
129-132 °C(lit.)
Molecular Formula
C10H12O4
Molecular Weight
196.200
Flash Point
138.6±15.8 °C
Exact Mass
196.073563
PSA
66.76000
LogP
2.91
Vapour Pressure
0.0±0.8 mmHg at 25°C
Index of Refraction
1.567
InChIKey
UQSRXQMIXSZGLA-UHFFFAOYSA-N
SMILES
CCOC(=O)c1c(C)cc(O)cc1O
Safety Information
Symbol
GHS07
Signal Word
Warning
Hazard Statements
H315-H319-H335
Precautionary Statements
P261-P305 + P351 + P338
Personal Protective Equipment
dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes
Xi: Irritant;
Risk Phrases
R36/37/38
Safety Phrases
S26-S37/39
RIDADR
NONH for all modes of transport
WGK Germany
3
HS Code
2918199090
Customs
HS Code
2918199090
Summary
2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%
Articles2
More Articles
In vitro evaluation of the antimicrobial activity of lichen metabolites as potential preservatives.
Antimicrobial screening of several lichen species and subsequent isolation and structure elucidation of active compounds revealed that the hydrolysis products of certain lichen metabolites, i.e., deps...
Antibacterial activity of orsellinates. Gomes AT, et al.