1,3-Bis(4-aminophenyl)adamantane - Names and Identifiers
Name | 1,3-Bis(4-aminophenyl)adamantane
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Synonyms | 1,3-Bis(p-aminophenyl)adamantane 1,3-Bis(4-aminophenyl)adamantane 1,3-Bis(4-PhenylaMino)AdaMantane 4,4'-(Adamantane-1,3-diyl)dianiline 4,4'-Tricyclo[3.3.1.13,7]decane-1,3-diylbisbenzenamine Benzenamine, 4,4'-tricyclo[3.3.1.13,7]decane-1,3-diylbis-
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CAS | 58788-79-7
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1,3-Bis(4-aminophenyl)adamantane - Physico-chemical Properties
Molecular Formula | C22H26N2
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Molar Mass | 318.46 |
Density | 1.215 |
Boling Point | 510.2±50.0 °C(Predicted) |
pKa | 5.09±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Sensitive | Irritant |
MDL | MFCD01826934 |
Use | Electronic materials or intermediates
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1,3-Bis(4-aminophenyl)adamantane - Introduction
1,3-Bis(4-aminophenyl)adamantane is an organic compound with the chemical formula C26H26N2. Its molecular structure contains an adamantane skeleton in which two benzene rings are linked together by amino groups. This compound has a number of interesting properties.
Nature:
1,3-Bis(4-aminophenyl)adamantane is a solid, colorless crystal at room temperature. It has a high melting point and thermal stability. The compound is insoluble in water, but is soluble in some organic solvents, such as methylene chloride or benzene.
Use:
1,3-Bis(4-aminophenyl)adamantane has important applications in the field of organic synthesis. It can be used as catalysts, complexes and functional materials synthesis intermediates. Its benzene ring structure enables it to form stable bonds with other compounds, resulting in excellent reactivity and special physical properties. In addition, it has been investigated as a modeling tool for drug molecules and dye materials.
Preparation Method:
The preparation of 1,3-Bis(4-aminophenyl)adamantane is usually accomplished by a multi-step reaction. The most common method is by oxidation of the disubstituted benzene ring on adamantane followed by reduction to produce the target product. The specific synthetic route can be adjusted according to the needs and chemical conditions of the study.
Safety Information:
There is no detailed report on the safety information of 1,3-Bis(4-aminophenyl)adamantane. However, according to general safety principles, dust contact or inhalation of the compound should be avoided. Appropriate protective gloves and glasses should be worn during operation to avoid direct contact with skin or eyes. In addition, the compound should be operated in a well-ventilated laboratory environment to avoid the accumulation of harmful gases.
Last Update:2024-04-09 21:54:55