191659-88-8
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Basic information
- Product Name: 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-
- Synonyms: 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-
- CAS NO:191659-88-8
- Molecular Formula: C10H18 O4
- Molecular Weight: 0
- EINECS: N/A
- Product Categories: N/A
- Mol File: 191659-88-8.mol
- Article Data: 0
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-(CAS DataBase Reference)
- NIST Chemistry Reference: 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-(191659-88-8)
- EPA Substance Registry System: 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-(191659-88-8)
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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: 191659-88-8(Hazardous Substances Data)
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Explanation
Different sources of media describe the Explanation of 191659-88-8 differently. You can refer to the following data:1. A spiroketal compound is a type of cyclic compound that contains a tetrahedral spiro center, which is a central carbon atom bonded to four different carbon atoms.
3. Cyclic ether ring
2. The compound has a cyclic ether ring, which is a closed loop of atoms containing an oxygen atom that forms a covalent bond with two carbon atoms.
4. Tetrahedral spiro center
3. The tetrahedral spiro center is a carbon atom that is bonded to four different carbon atoms, forming a three-dimensional structure.
5. Derivative of jiadifenolide
4. Jiadifenolide is a natural product isolated from plants, and the compound in question is a derivative of this natural product, meaning it has a similar structure but with some modifications.
6. 5-methoxy group
7. Potential pharmaceutical or biological applications
5. Due to the various biological activities found in spiroketal compounds, 1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)may have potential uses in the pharmaceutical or biological industries.
6. The stereochemistry of the compound is described by the relative positions of the atoms in space. In this case, the stereochemistry is defined by the (4.alpha.,5.alpha.,6.beta.) notation, which indicates the specific arrangement of the atoms at the 4th, 5th, and 6th positions in the molecule.
Stereochemistry
(4.alpha.,5.alpha.,6.beta.)Check Digit Verification of cas no
The CAS Registry Mumber 191659-88-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,6,5 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.Calculate Digit Verification of CAS Registry Number 191659-88:
(8*1)+(7*9)+(6*1)+(5*6)+(4*5)+(3*9)+(2*8)+(1*8)=178
178 % 10 = 8
So 191659-88-8 is a valid CAS Registry Number.
191659-88-8Upstream product
191659-88-8Downstream Products
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1,7-Dioxaspiro5.5undecan-4-ol, 5-methoxy-, (4.alpha.,5.alpha.,6.beta.)-
