134110-57-9 Usage
Chemical structure
A spirocyclic molecule with a tetraoxaspiro[4.4]nonane core and two phenyl groups attached at the 2 and 7 positions.
Molecular weight
Approximately 304.35 g/mol
Appearance
It is likely a colorless or white crystalline solid, although the exact appearance may vary depending on the specific synthesis and purification methods used.
Solubility
The solubility of 1,4,6,9-Tetraoxaspiro[4.4]nonane, 2,7-diphenylis not explicitly mentioned in the provided material. However, due to its nonpolar nature and the presence of phenyl groups, it is likely to be more soluble in organic solvents such as dichloromethane, ethyl acetate, or toluene, rather than in water.
Stability
The stability of 1,4,6,9-Tetraoxaspiro[4.4]nonane, 2,7-diphenylis not explicitly mentioned in the provided material. However, as a general rule, spirocyclic compounds tend to be relatively stable due to the strain in the ring system, which makes them less prone to undergo reactions that would break the ring.
Reactivity
1,4,6,9-Tetraoxaspiro[4.4]nonane, 2,7-diphenylis commonly used as a building block in organic synthesis and drug development, indicating that it is likely to be reactive with various reagents and undergo a range of chemical reactions, such as electrophilic aromatic substitution on the phenyl groups or nucleophilic attack on the carbon atoms in the spiro ring.
Applications
It has been studied for its potential applications in pharmaceuticals, including as a precursor to molecules with biological activity.
Research interest
Its unique structure and properties make it an interesting target for chemical research and development in various industries.
Safety and handling
The safety and handling information for 1,4,6,9-Tetraoxaspiro[4.4]nonane, 2,7-diphenylis not provided in the material. However, as with any chemical compound, it is essential to follow proper safety protocols, including wearing appropriate personal protective equipment (PPE) and using proper ventilation when handling 1,4,6,9-Tetraoxaspiro[4.4]nonane, 2,7-diphenyl-.
Check Digit Verification of cas no
The CAS Registry Mumber 134110-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134110-57:
(8*1)+(7*3)+(6*4)+(5*1)+(4*1)+(3*0)+(2*5)+(1*7)=79
79 % 10 = 9
So 134110-57-9 is a valid CAS Registry Number.
134110-57-9Relevant academic research and scientific papers
Activation and Control of the Reaction of the Reaction of Dioxastannolane with Carbon Disulfide and Phenyl Isothiocyanate by the Addition of Bases
Yano, Katsunori,Baba, Akio,Matsuda, Haruo
, p. 1881 - 1884 (2007/10/02)
1,3-Dioxa-2-stannolanes 1 are readily activated by Lewis bases such as Bu3P and Et3N to give cycloadducts on reaction with carbon disulfide or phenyl isothiocyanate under mild conditions.In particular, bases play a characteristic role in the reaction with
