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Coumestrol

Catalog No. 27883 Name Sigma Aldrich
CAS Number 479-13-0 Website http://www.sigmaaldrich.com
M. F. C15H8O5 Telephone 1-800-521-8956
M. W. 268.22102 Fax
Purity ≥97.5% (HPLC) Email
Storage Chembase ID: 126724

SYNONYMS

IUPAC name
5,14-dihydroxy-8,17-dioxatetracyclo[8.7.0.02,7.011,16]heptadeca-1(10),2,4,6,11(16),12,14-heptaen-9-one
IUPAC Traditional name
coumestrol
Synonyms
7,12-Dihydroxycoumestan

DATABASE IDS

CAS Number 479-13-0
MDL Number MFCD00016885
Beilstein Number 266702
PubChem SID 24856835
EC Number 207-525-6

PROPERTIES

Empirical Formula (Hill Notation) C15H8O5
Product Line BioReagent
Purity ≥97.5% (HPLC)
Suitability suitable for fluorescence
Gene Information human ... ESR1(2099), ESR2(2100)mouse ... Esr1(13982)rat ... Ar(24208)
Fluorescence λex 377 nm; λem 437 nm in 0.1 M Tris pH 8.0
Melting Point ≥350 °C(lit.)
Solubility DMSO: soluble
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302-H315-H319-H335
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 22-36/37/38
RTECS DF8077000
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Coumestrol has anti-estrogenic actions in the brain and pituitary, mediated through estrogen receptor-α.1
Description (简体中文)
Biochem/physiol Actions
Coumestrol has anti-estrogenic actions in the brain and pituitary, mediated through estrogen receptor-α.1

REFERENCES