3as 3aalpha 6alpha 7abeta Hexahydro 8 8 Dimethyl 3h 3a 6 Methano 2 1 Benzisothiazole 2 2 Dioxide
Quinoline Thiophene Imidazole Thiazole
[3aS-(3aalpha,6alpha,7abeta)]-Hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
Chemical Name [3aS-(3aα,6α,7aβ)]-Hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide
Molecular Formula C11H17NO2S
Molecular Weight 227.323 g/mol
Physical State Solid (usually)
Melting Point Typically in a specific range (data needed for exact value)
Boiling Point Typically in a specific range (data needed for exact value)
Solubility Solubility characteristics depend on solvent (data needed for specific solvents)
Density Value needed for exact density
Odor Odor information required
Color Color information required
Pka pKa value needed
FAQ

What is [3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methano-2,1-benzisothiazole 2,2-dioxide?

[3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide is an organic compound. It has a specific chemical structure and is composed of hexahydro, dimethyl and specific benzoisothiazole structures and dioxide functional groups.

In the structure of this compound, the hexahydro part contains multiple saturated carbon-carbon bonds, which are arranged in a cyclic arrangement, giving it a certain stability and spatial configuration. The substituent of 8,8-dimethyl affects the steric resistance and physicochemical properties of the molecule, and changes its polarity and solubility. The 3a, 6-methylene moiety forms a unique bridge ring structure in the benzoisothiazole ring system, which has a significant effect on the reactivity and stereochemical characteristics of the compound. The benzoisothiazole structure provides a specific electron cloud distribution and reaction check point for the molecule, while the 2,2-oxide functional group enhances the hydrophilicity and oxidation of the molecule.

In the field of organic chemistry, such compounds may exhibit biological activity in the field of medicinal chemistry due to their unique structures. As potential drug lead compounds, they interact with specific targets in organisms to exert therapeutic effects. In the field of materials science, its structural properties may endow materials with special electrical, optical or mechanical properties, which can be used to prepare special functional materials.

What is the chemical structure of [3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methano-2,1-benzisothiazole 2,2-dioxide?

[3aS- (3aα, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide, this is an organic compound. Its chemical structure is complex and contains a core skeleton of benzoisothiazole. This skeleton is formed by fusing a benzene ring with an isothiazole ring, giving the compound unique chemical activity and stability.

The hexahydro-8,8-dimethyl part indicates that the compound has six hydrogen atoms in a specific position, and is connected to a methyl group at each of the two positions numbered 8. The presence of this methyl group affects the spatial structure and electron cloud distribution of the molecule, which in turn affects the physical and chemical properties of the compound.

The 3a, 6-methylene moiety means that a methylene bridge is formed between the 3a and 6 positions, which changes the topology of the molecule and increases the rigidity and stability of the molecule.

2,2-Dioxide refers to the double bond between the sulfur atom and the two oxygen atoms in the isothiazole ring. This structure significantly enhances the oxidation and reactivity of the compound, which makes the compound exhibit unique properties in many chemical reactions and biological processes.

The chemical structure of this compound is unique, and the interaction of each part jointly determines its physical, chemical and biological activities, which lays the foundation for its application in pharmaceutical chemistry, materials science and other fields.

What are the physical properties of [3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methano-2,1-benzisothiazole 2,2-dioxide?

[3aS- (3aα, 6α, 7aβ) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide, this substance has the following physical properties:

Its appearance is often white to white-like crystalline powder, like finely crushed jade chips, delicate and uniform. The melting point range is in a specific range, about [X] ℃ - [X] ℃, just like the nature of things, this melting point is its inherent characteristic, and it changes when heated. When it reaches this temperature limit, it begins to melt.

This substance is almost insoluble in water, just like the opposite of oil and water, the two are difficult to blend. However, in organic solvents, it has different behaviors, slightly soluble in ethanol, like snowflakes falling in alcohol solution, slightly dispersed; slightly better solubility in dichloromethane, able to disperse and dissolve to a certain extent, just like light dust falling in it, gradually fading.

Its density is also an important physical property, about [X] g/cm ³, and the texture is light and heavy. Compared with other substances, it can be judged from this density value.

The stability of this substance is acceptable. Under normal environmental conditions, such as room temperature and pressure, its properties do not change rapidly, just like a state of stability. In case of extreme conditions such as strong oxidizing agents or high temperatures, chemical reactions may also occur, the structure may change, and the physical properties may change accordingly.

What are the chemical properties of [3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methano-2,1-benzisothiazole 2,2-dioxide?

This is [3aS- (3aα, 6α, 7aβ) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide, and its chemical properties are quite unique.

This compound has certain stability, and the benzoisothiazole ring in the molecular structure is connected to hexahydro and methylene parts, giving it specific chemical activity. Because it contains sulfur atoms and is in a dioxide state, it can participate in the reaction as a sulfur source in some chemical reactions, exhibiting unique chemical behaviors.

In terms of electron cloud distribution, the electron migration between different atoms in its structure makes some parts electrophilic or nucleophilic. For example, the benzene ring part has certain electron delocalization characteristics due to the existence of a conjugated system, and is easy to react with electrophilic reagents. The saturated carbon chain part such as methylene is relatively stable, but under appropriate conditions, such as high temperature and the presence of strong oxidants, reactions such as oxidation may also occur.

In addition, the dimethyl group in this compound will affect the electron cloud density distribution of the whole molecule due to the electron supply effect of methyl, which in turn affects its chemical activity and reaction selectivity. In the field of organic synthesis, according to its chemical properties, its structure can be modified and modified through specific reactions to prepare new compounds with specific functions.

What is the main use of [3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methano-2,1-benzisothiazole 2,2-dioxide?

[3aS- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide, this compound has important uses in many fields.

In the field of medicine, it may have unique pharmacological activities. Or it can act on specific biological targets, and precisely bind to biomolecules in the body to produce regulatory effects on specific physiological processes, such as participating in the regulation of cell signaling pathways, thereby providing new strategies for disease treatment, or developing innovative drugs for specific diseases.

In the field of materials science, the special structure of this compound gives it unique physicochemical properties. Or it can be integrated into the material system as a functional additive to improve the stability, durability or other key properties of the material. For example, it is added to polymer materials to improve the anti-aging, chemical corrosion resistance and other properties of the material, and broaden the application range of the material in complex environments.

In the field of agriculture, or with potential biological activity, it can be used to develop new pesticides. By virtue of the interference effect on the specific physiological mechanism of pests, high-efficiency and low-toxicity pest control can be achieved, providing strong support for the sustainable development of agriculture.

In addition, in the field of fine chemicals, it may be used as an important intermediate to synthesize compounds with more complex structures and more unique functions, promoting the diversified development of fine chemical products and meeting the needs of different industries for special chemicals.