(3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate is a chemical compound with the molecular formula C30H46O4, belonging to the class of organic peroxides and being a derivative of lanosterol, a precursor of cholesterol. (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate is typically found in plants and is believed to possess potential biological activities, such as anti-inflammatory and anti-tumor properties. The hydroperoxide group in its structure contributes to its reactive nature, enabling it to engage in various chemical reactions, while the acetate group provides relative stability to the compound. This stability, along with its potential biological activities, suggests possible applications in the pharmaceutical industry and other areas. However, further research is necessary to fully comprehend and utilize the properties and potential uses of (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate.
19666-89-8
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Basic information
- Product Name: (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate
- Synonyms:
- CAS NO:19666-89-8
- Molecular Formula: C32H54O4
- Molecular Weight: 502.7688
- EINECS: N/A
- Product Categories: N/A
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 558.1°C at 760 mmHg
- Flash Point: 165.2°C
- Appearance: N/A
- Density: 1.04g/cm3
- Vapor Pressure: 8.78E-15mmHg at 25°C
- Refractive Index: 1.521
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate(CAS DataBase Reference)
- NIST Chemistry Reference: (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate(19666-89-8)
- EPA Substance Registry System: (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate(19666-89-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 19666-89-8(Hazardous Substances Data)
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19666-89-8 Usage
Uses
Used in Pharmaceutical Industry:(3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate is used as a potential therapeutic agent for its anti-inflammatory and anti-tumor properties. (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate's reactive hydroperoxide group may play a role in modulating biological responses, making it a candidate for the development of new drugs targeting inflammation and cancer.
Used in Chemical Research:
In the field of chemical research, (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate can be used as a starting material or a model compound for studying the reactions and properties of organic peroxides and their derivatives. This may lead to the discovery of new chemical reactions or the development of novel compounds with specific applications.
Used in Drug Delivery Systems:
Similar to other biologically active compounds, (3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate could be incorporated into drug delivery systems to improve its bioavailability and targeting to specific tissues or cells. This application would require further investigation into the compound's pharmacokinetics and potential interactions with biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 19666-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,6 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.Calculate Digit Verification of CAS Registry Number 19666-89:
(7*1)+(6*9)+(5*6)+(4*6)+(3*6)+(2*8)+(1*9)=158
158 % 10 = 8
So 19666-89-8 is a valid CAS Registry Number.
19666-89-8Upstream product
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(3beta,7beta)-7-hydroperoxylanost-8-en-3-yl acetate
