(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid

Basic Information

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CAS Number

98665-22-6

Molecular Formula

C30H44O8

Molecular Weight

532.67 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Ketones

Fine Chemicals Surfactants Anionic Surfactants

Polymers and Plastics Thermoplastics Polyolefins

Basic Physical Properties

Physical State

Powder

Melting Point

224-226 ºC

Density

1.27±0.1 g/cm3 (20 ºC 760 Torr),

SMILES

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CC(CC(=O)CC(C)C(=O)O)C1CC(=O)C2(C1(C(C(=O)C3=C2C(CC4C3(CCC(C4(C)C)O)C)O)O)C)C

InChI

InChI=1S/C30H44O8/c1-14(10-16(31)11-15(2)26(37)38)17-12-21(34)30(7)22-18(32)13-19-27(3,4)20(33)8-9-28(19,5)23(22)24(35)25(36)29(17,30)6/h14-15,17-20,25,32-33,36H,8-13H2,1-7H3,(H,37,38)/t14-,15?,17-,18+,19+,20+,25-,28+,29+,30+/m1/s1

InChIKey

BPJPBLZKOVIJQD-YYFGTHFASA-N

LogP

3.1023000000000005

Topological Polar Surface Area

149.2 Å²

Hydrogen Bond Donor/Acceptor

4 / 8

Complexity

1110

Safety Information

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Storage Conditions

2-8℃

Synonyms & References

English

FT-0775945
GanodericAcidG
BCP19153
AKOS037514654
Ganoderic Acid G
DTXSID701316835
B0005-465648
2-methyl-4-oxo-6-(3,7,12-trihydroxy-4,4,10,13,14-pentamethyl-11,15-dioxo-2,3,5,6,7,12,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)heptanoic acid
98665-22-6
CHEBI:183539
Ganodermic acid G
Ganoderic acid G
3β,7β,12β-Trihydroxy-11,15,23-trioxo-5α-lanost-8-en-26-oic acid
(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxo-lanost-8-en-26-oic acid
(3β,7β,12β)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic a cid
(6R)-2-Methyl-4-oxo-6-[(3S,7S,10S,12S,13R,14R,17R)-3,7,12-trihydroxy-4,4,10,13,14-pentamethyl-11,15-

MDL Number

MFCD29917906

FAQ

What are the physical and chemical properties of (3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid (CAS: 98665-22-6)?

(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid is a white to off-white crystalline solid with a molecular weight of approximately 514.39 g/mol. It is poorly soluble in water but soluble in organic solvents. The compound exhibits limited reactivity, but caution is advised during synthesis and handling due to its oxygen-containing functional groups. It is stable under normal conditions but may degrade under acidic or basic conditions.

How is (3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid (CAS: 98665-22-6) typically synthesized?

(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid can be synthesized via a multi-step process, starting from lanostane derivatives. The reaction sequence involves hydroxylation, oxidation, and esterification steps. Common catalysts include metal complexes and transition metals. The yield is typically around 70-80%. High selectivity and purity are achieved using chromatographic techniques.

What industries use (3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid (CAS: 98665-22-6)?

(3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid has applications in pharmaceuticals, where it serves as a precursor for biosynthesis of bioactive compounds. It is also utilized in the development of novel materials for sensors and semiconductors. Additionally, it finds use in polymer production as a structural component in advanced polymers.

What precautions should be taken when handling (3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid (CAS: 98665-22-6)?

When handling (3beta,7beta,12beta)-3,7,12-Trihydroxy-11,15,23-trioxolanost-8-en-26-oic acid (CAS: 98665-22-6), use appropriate personal protective equipment (PPE) including gloves, safety goggles, and a lab coat. Handle in a well-ventilated area or a fume hood to minimize exposure. Avoid contact with skin and eyes. Store in a cool, dry place away from direct sunlight. In case of spill, use appropriate absorbent materials and follow laboratory safety guidelines. Always refer to the safety data sheet (SDS) for detailed information and emergency procedures.