ELEUTHEROSIDE C

Basic Information

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CAS Number

15486-24-5

Molecular Formula

C8H16O6

Molecular Weight

208.21 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Ethers

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Basic Physical Properties

Physical State

Powder

SMILES

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CCOC1C(C(C(C(O1)CO)O)O)O

InChI

InChI=1S/C8H16O6/c1-2-13-8-7(12)6(11)5(10)4(3-9)14-8/h4-12H,2-3H2,1H3/t4-,5+,6+,7-,8+/m1/s1

InChIKey

WYUFTYLVLQZQNH-HNEXDWKRSA-N

LogP

-2.177199999999999

Topological Polar Surface Area

99.38000000000001 Å²

Hydrogen Bond Donor/Acceptor

4 / 6

Complexity

175

Synonyms & References

English

CS-0024249
HY-N3802
Ethyl -D-galactoside;Ethyl -D-galactopyranoside
ethyl a-d-galactopyranoside
(2S,3R,4S,5R,6R)-2-ETHOXY-6-(HYDROXYMETHYL)OXANE-3,4,5-TRIOL
MS-23142
ELEUTHEROSIDE C
SCHEMBL2446115
?-D-GALACTOPYRANOSIDE, ETHYL
AKOS032948775
ELEUTHEROSIDEC
15486-24-5
DTXSID50879263
Ethyl a-D-galactoside
a-D-Galactopyranoside, ethyl
Eleutheroside C
Ethyl a-D-galactopyranoside
Galactopyranoside,ethyl (7CI)
Ethyl α-D-galactopyranoside
Ethyl glucoside
Ethyl D-glucoside
2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
(2R,3R,4S,5R,6R)-2-Ethoxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
beta-D-Glucopyranoside, ethyl
ethylD-glucoside
octyl-d-glucoside
(2S,3R,4S,5S,6R)-2-Ethoxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
AK104307
(3R,4S,5S,6R)-2-ethoxy-6-(hydroxymethyl)oxane-3,4,5-triol
(-)-Ethyl beta-D-glucopyranoside
NSC229294

MDL Number

MFCD03427298

FAQ

What are the physical and chemical properties of ELEUTHEROSIDE C (CAS: 15486-24-5)?

ELEUTHEROSIDE C is a white crystalline compound with a molecular weight of approximately 578.42. It has limited solubility in water but is soluble in organic solvents. Chemically, it is relatively stable under normal conditions but can react with strong acids. Its crystal structure is monoclinic.

How is ELEUTHEROSIDE C (CAS: 15486-24-5) typically synthesized?

ELEUTHEROSIDE C is synthesized via a complex multistep process involving glycosylation reactions. Commonly, it is prepared from the saponification of eleutherococcus root extracts. The synthesis involves the use of specific catalysts and solvents to achieve good yields and high selectivity.

What industries use ELEUTHEROSIDE C (CAS: 15486-24-5)?

ELEUTHEROSIDE C is primarily used in the pharmaceutical industry for its potential health benefits. It is also explored in the cosmetics industry for its antioxidant properties. Its chemical structure makes it useful in developing new drug candidates and as a natural ingredient in personal care products.

What precautions should be taken when handling ELEUTHEROSIDE C (CAS: 15486-24-5)?

When handling ELEUTHEROSIDE C, ensure proper personal protective equipment (PPE) such as gloves, goggles, and laboratory coat. Store it in a cool, dry place away from direct sunlight and other chemicals. In case of a spill, use appropriate spill kits and follow the safety data sheet (SDS) for disposal. Always work in a well-ventilated area or fume hood.