1 3 Dihydro 3 3 Iodopropyl 7 8 Dimethoxy 2h 3 Benzazepin 2 One
Iodobenzene

1,3-dihydro-3-(3-iodopropyl)-7,8-dimethoxy-2h-3-benzazepin-2-one

Fengxi Chemical

Specifications

HS Code

314246

Chemical Formula C16H20INO4
Molecular Weight 403.24
Appearance Solid (usually)
Solubility In Water Low (organic compound with non - polar parts)
Solubility In Organic Solvents Soluble in some organic solvents like chloroform, dichloromethane
Odor Odorless (usually for such non - volatile solids)
Color Colorless to white (typical for pure solid organic compounds)
Logp Calculated value would indicate lipophilicity due to alkyl and aromatic groups
Chemical Name 1,3 - dihydro - 3 - (3 - iodopropyl)-7,8 - dimethoxy - 2H - 3 - benzazepin - 2 - one
Molecular Formula C16H20INO3
Molecular Weight 399.24
Physical State Solid (predicted, based on similar compounds)
Solubility Soluble in organic solvents like chloroform, dichloromethane (predicted from its non - polar aromatic and moderately polar functional groups), less soluble in water
Logp Positive value (indicating lipophilicity, likely around 2 - 4 based on similar structures with alkoxy and alkyl - iodide groups)
Color Colorless to pale yellow solid (predicted from related compounds with similar functional groups)
Chemical Formula C16H20INO4
Molecular Weight 403.24
Chemical Formula C16H20INO4
Molecular Weight 403.24
Iupac Name 3-(3-iodopropyl)-7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one
Physical State Solid (predicted)
Solubility In Water Low (predicted due to non - polar nature of the molecule)
Logp Estimated to be moderately lipophilic
Appearance Colorless to light - colored solid (predicted)
Packing & Storage
Packing 100g of 1,3 - dihydro - 3-(3 - iodopropyl)-7,8 - dimethoxy - 2H - 3 - benzazepin - 2 - one in sealed chemical - grade vial.
Storage 1,3 - dihydro - 3 - (3 - iodopropyl)-7,8 - dimethoxy - 2H - 3 - benzazepin - 2 - one should be stored in a cool, dry place away from direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and potential reaction with air components. Store it separately from incompatible substances, and ensure the storage area has proper ventilation to avoid the build - up of harmful vapors.
Shipping The chemical 1,3 - dihydro - 3 - (3 - iodopropyl)-7,8 - dimethoxy - 2H - 3 - benzazepin - 2 - one should be shipped in properly sealed, corrosion - resistant containers. Ensure compliance with hazardous chemical shipping regulations for safe transit.
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1,3-dihydro-3-(3-iodopropyl)-7,8-dimethoxy-2h-3-benzazepin-2-one 1,3-dihydro-3-(3-iodopropyl)-7,8-dimethoxy-2h-3-benzazepin-2-one 1,3-dihydro-3-(3-iodopropyl)-7,8-dimethoxy-2h-3-benzazepin-2-one
General Information
Frequently Asked Questions
What are the chemical properties of 1,3 - dihydro - 3 - (3 - iodopropyl) -7,8 - dimethoxy - 2h - 3 - benzazepin - 2 - one
1%2C3+-+dihydro+-+3+-+%283+-+iodopropyl%29-7%2C8+-+dimethoxy+-+2h+-+3+-+benzazepin+-+2+-+one is an organic compound with specific chemical properties.
Looking at its structure, the compound has high polarity due to the iodine atom above the propyl group. The presence of iodine atoms enhances the intermolecular force, or affects its melting and boiling point and solubility. Usually, the melting and boiling point of iodine-containing organic compounds is relatively high, because the iodine atom has a large relative atomic weight and the intermolecular dispersion force is enhanced. In terms of solubility, due to the increase in polarity, it has good solubility in polar solvents such as alcohols and ketones, and poor solubility in non-polar solvents such as alkanes.
Furthermore, the structure of benzazalone in the molecule gives it unique chemical activity. This structure is common in many bioactive molecules, or has potential biological activity. For example, it may interact with specific targets in vivo, or involve the field of drug research and development. It can be used as a lead compound to modify drugs with specific pharmacological activities.
The methoxy group in the molecule also affects its chemical properties. Methoxy group is the power supply subgroup, which can increase the electron cloud density of the benzene ring, change the electrophilic substitution activity of the benzene ring, and make it more prone to electrophilic substitution reactions. The substitution position or the methoxy group localization effect is affected, and it mostly occurs in the methoxy group ortho-para-position.
Overall, the chemical properties of 1%2C3+-+dihydro+-+3+-+%283+-+iodopropyl%29-7%2C8+-+dimethoxy+-+2h+-+3+-+benzazepin+-+2+-+one are determined by the interaction of various groups in the molecule, and may have important research value and application potential in the fields of organic synthesis and medicinal chemistry.
What are the main uses of 1,3 - dihydro - 3 - (3 - iodopropyl) -7,8 - dimethoxy - 2h - 3 - benzazepin - 2 - one
1%2C3+-+dihydro+-+3+-+%283+-+iodopropyl%29-7%2C8+-+dimethoxy+-+2h+-+3+-+benzazepin+-+2+-+one, this is the name of an organic compound. This compound is useful in both the pharmaceutical and chemical fields.
In the field of medicine, or involved in drug development. In some drug development processes, compounds with specific structures need to be used as starting materials or intermediates. By modifying and modifying their chemical structures, new compounds with specific pharmacological activities can be obtained for the treatment of diseases. For example, in the development of drugs for neurological diseases, the compound or due to a specific chemical structure, can be properly transformed to obtain substances that have specific effects on neurotransmitter receptors, or help improve the symptoms of neurological-related diseases.
In the chemical field, or in the synthesis of materials. Due to its unique chemical structure, it can participate in the polymerization reaction as a functional monomer. After polymerization with other monomers, polymer materials with special properties can be prepared, such as materials with specific solubility, thermal stability or optical properties, which can be used for the improvement of coatings, plastics and other materials to meet the needs of different industrial production.
With its unique chemical structure, this compound has shown potential and important uses in pharmaceutical research and development and chemical material synthesis, providing a material basis and possibility for the development of related fields.
What is the synthesis method of 1,3 - dihydro - 3 - (3 - iodopropyl) -7,8 - dimethoxy - 2h - 3 - benzazepin - 2 - one
To prepare 1% 2C3-dihydro-3- (3-iodopropyl) -7% 2C8-dimethoxy-2h-3-benzazepin-2-one, the method is as follows:
Take 7,8-dimethoxy-3-isobutylenyl-2-benzazepine-2-one as the starting material and dissolve it in an appropriate amount of organic solvent, such as dichloromethane or the like, because dichloromethane has good solubility to the raw material and is relatively stable in nature, which is convenient for subsequent reactions.
Then, slowly add iodine-containing reagents to it, such as a mixture of iodine elemental substance and a suitable oxidant, commonly used oxidants such as hydrogen peroxide, etc. The dropwise addition process requires strict control of the speed and temperature to prevent the reaction from being too violent. Usually the temperature is maintained at 0-10 ° C. This low temperature environment can make the reaction proceed smoothly and reduce the occurrence of side reactions.
After the dropwise addition is completed, heat up to room temperature and continue to stir to make the reaction sufficient. The reaction process should be closely monitored at this stage. By means of thin layer chromatography, etc., when the raw material point disappears, the reaction is basically completed.
Next, the reaction solution is post-treated. Wash with an appropriate amount of water to remove unreacted water-soluble impurities, and separate the liquid to take the organic phase. Then dry the organic phase with a desiccant such as anhydrous sodium sulfate to remove the moisture in it.
Finally, the organic solvent is removed by reduced pressure distillation to obtain a crude product. Further purification by column chromatography and other methods can obtain a pure 1% 2C3 - dihydro - 3- (3 - iodopropyl) -7% 2C8 - dimethoxy - 2h - 3 - benzazepin - 2 - one product. It should be noted that the operation process should be carried out in a well-ventilated environment and strictly follow the safety regulations of chemical experiments to ensure experimental safety and accurate results.
1,3 - dihydro - 3 - (3 - iodopropyl) -7,8 - dimethoxy - 2h - 3 - benzazepin - 2 - one what is the market outlook
1%2C3+-+dihydro+-+3+-+%283+-+iodopropyl%29-7%2C8+-+dimethoxy+-+2h+-+3+-+benzazepin+-+2+-+one, this is the chemical name of an organic compound, but its appearance in the market prospect is now described in the style of the ancient Chinese saying of "Tiangong Kaiwu".
Looking at this compound today, although it has not been widely used in the market at present, it has a unique chemical structure or hidden potential. Looking at all things in the world, it starts at the end of the micro and gradually becomes a big view. The synthesis of this compound requires exquisite methods and pure materials to obtain its good products.
Although its market has not yet been widely expanded, the way of chemistry is changing with each passing day. In time, if the unique properties of this compound can be explored, it may find a place for use in medicine, materials and other fields. Like the craftsmen of ancient times, they study their skills carefully, and they will be used by the world as soon as they acquire the method.
At present, the wind of scientific research is booming, and scholars are diligent in their research, or in the near future, they will be able to understand the wonderful use of this compound, making it stand out in the market, like a pearl in the dust, glowing. Although its market prospect is uncertain, the future road is full of variables and opportunities. We should wait for its development to change with diligence and exploration.
1,3 - dihydro - 3 - (3 - iodopropyl) -7,8 - dimethoxy - 2h - 3 - benzazepin - 2 - one What are the precautions during use
1% 2C3 - dihydro - 3 - (3 - iodopropyl) -7% 2C8 - dimethoxy - 2h - 3 - benzazepin - 2 - one is an organic compound. When using, many precautions must be observed.
First, this substance is chemically active. When contacting, be careful not to contact the skin and eyes. If you accidentally touch the skin, rinse with plenty of water as soon as possible and seek medical attention as appropriate; if it enters the eye, rinse with water immediately and then seek medical help urgently. Second, the ventilation of the use environment must be good. Because it may evaporate certain gases, if the ventilation is poor, the gas will accumulate, or it will cause health risks, such as respiratory discomfort, dizziness, etc.
Furthermore, attention should also be paid to storage. It should be placed in a cool, dry place, away from fire sources and oxidants. The chemical properties of this compound may change due to factors such as temperature and humidity, oxidation, etc. Improper storage, or loss of its effectiveness, or even danger. Fourth, during use, the cleaning and adaptation of the experimental equipment is crucial. Unclean equipment or impurities mixed in, affecting the reaction or product purity; unsuitable equipment or unable to achieve the expected experimental conditions.
In addition, the amount of this compound should be precisely controlled. Excessive use, or cause the reaction to go out of control, the product is not pure; insufficient dosage, it is difficult to achieve the desired effect. And the use of personnel should be familiar with its chemical properties and safety procedures, untrained people should not operate without authorization, so as not to cause trouble. In short, when using this product, all aspects need to be cautious to ensure safety and effectiveness.