4-(4-trans-Vinyl-[1,1′-bicyclohexyl]-4′-trans-yl)-1,2-difluorbenzol - Names and Identifiers
Name | trans-4-(3,4-Difluorophenyl)-trans-4'-vinylbicyclohexane
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Synonyms | -4-(3,4-Difluorophenyl) -4'-vinyl-1,1'-bi(cyclohexane) 4-(3,4-difluorophenyl)-4'-vinylbi(cyclohexane) trans,trans-4-(3,4-Difluorophenyl)-4'-vinylbicyclohexyl trans-4-(3,4-Difluorophenyl)-trans-4'-vinylbicyclohexane TRANS,TRANS-4-(3,4-DIFLUORO-PHENYL)-4'-VINYL-BICYCLOHEXYL (trans,trans)-4-(3,4-Difluorophenyl)-4'-vinyl-1,1'-bi(cyclohexane) 4-(4-trans-Vinyl-[1,1′-bicyclohexyl]-4′-trans-yl)-1,2-difluorbenzol 4-[(trans,trans)-4'-Ethenyl[1,1'-bicyclohexyl]-4-yl]-1,2-difluorobenzene
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CAS | 142400-92-8
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InChI | InChI=1/C20H26F2/c1-2-14-3-5-15(6-4-14)16-7-9-17(10-8-16)18-11-12-19(21)20(22)13-18/h2,11-17H,1,3-10H2/t14-,15-,16?,17- |
4-(4-trans-Vinyl-[1,1′-bicyclohexyl]-4′-trans-yl)-1,2-difluorbenzol - Physico-chemical Properties
Molecular Formula | C20H26F2
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Molar Mass | 304.42 |
Density | 1.087±0.06 g/cm3(Predicted) |
Melting Point | 44.0 to 48.0 °C |
Boling Point | 368.0±42.0 °C(Predicted) |
Storage Condition | Inert atmosphere,Room Temperature |
Refractive Index | 1.545 |
4-(4-trans-Vinyl-[1,1′-bicyclohexyl]-4′-trans-yl)-1,2-difluorbenzol - Introduction
trans, trans-4-(3,4-difluorophenyl)-4 '-vinylbicyclohexane is a compound also known as Difluorobenzene-ethylene bridged dicyclohexane.
Nature:
Anti-, anti -4-(3,4-difluorophenyl)-4 '-vinyl bicyclohexane is a solid with special structure and properties. It is colorless and easily dissolves in organic solvents. It is highly stable and insensitive to light, heat and chemical reactions.
Use:
trans, trans-4-(3,4-difluorophenyl)-4 '-vinyl bicyclohexane has many uses in the chemical industry, mainly used as a catalyst or intermediate in organic synthesis reactions. It can be used in synthetic materials science, coordination chemistry, organic synthesis and other fields. It can also be used for the preparation of organic optoelectronic materials.
Preparation Method:
Anti-, anti -4-(3,4-difluorophenyl)-4 '-vinyl bicyclohexane has many preparation methods, the most commonly used method is to prepare by ring synthesis reaction. Specific steps involve reaction with a diene compound and an aromatic halide to form the target compound.
Safety Information:
The safety information for trans-4-(3,4-difluorophenyl)-4 '-vinyl bicyclohexane may vary by country. During handling, appropriate chemical laboratory procedures should be followed and appropriate personal protective measures should be taken, including wearing gloves, laboratory coats and goggles. Care should be taken to avoid inhalation, ingestion or contact with skin and eyes when using or handling the substance. In the event of an accident, medical assistance should be sought immediately.
Please note that the above information is for reference only. The specific preparation method and safe operation should be carried out according to the specific experimental conditions and laboratory safety guidelines.
Last Update:2024-04-09 19:05:46