21681-47-0

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms and 16 hydrogen (H) atoms.
2. Bicyclic compound

Explanation

A bicyclic compound is a type of organic molecule that contains two rings of carbon atoms. 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethanonaphthalene has two fused rings, which contribute to its unique structure and properties.
3. Terpene classification

Explanation

Terpenes are a large and diverse class of organic compounds that are produced by plants. They are often characterized by their strong, pleasant scents and are used in various industries, such as perfumery and the food industry.
4. Aromatic plant source

Explanation

1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethanonaphthalene is found in certain aromatic plants, which are plants that produce volatile organic compounds with strong, distinctive odors. These plants are often used for their scent in various applications.
5. Pleasant scent

Explanation

The compound is known for its pleasant and attractive scent, which makes it a valuable component in the production of perfumes and other fragrances.
6. Perfumery use
7. Flavoring agent in the food industry

Explanation

In addition to its use in perfumery, 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethanonaphthalene is also used as a flavoring agent in the food industry. Its pleasant scent can be used to enhance the taste and aroma of various food products.
8. Complex and unique structure

Explanation

The compound has a complex molecular structure, with multiple carbon and hydrogen atoms arranged in a specific pattern. This unique structure contributes to its properties and makes it valuable in various commercial applications.
9. Commercial applications

Explanation

Due to its properties, such as its pleasant scent and unique structure, 1,2,3,4,4a,5,8,8a-octahydro-2-methyl-1,4:5,8-dimethanonaphthalene has a wide range of commercial applications, including the production of perfumes, flavoring agents in the food industry, and potentially other uses in the chemical and pharmaceutical industries.

InChI:InChI=1/C13H18/c1-7-4-10-6-11(7)13-9-3-2-8(5-9)12(10)13/h2-3,7-13H,4-6H2,1H3

Upstream product

• 77-73-6 bi(cyclopentadiene) 
• 822-96-8 5-methylbicyclo[2.2.1]heptan-2-ene 
• 542-92-7 cyclopenta-1,3-diene 
• 822-96-8 5-methyl-2-norbornene 

Relevant academic research and scientific papers

Epoxidation of tetracyclodecene hydrocarbons with the H2O2·CO(NH2)2 adduct in the presence of heteropoly compounds containing rare-earth metal cations

Epoxidation of tetracyclododecene bridged hydrocarbons prepared via the [4+2]-condensation of bicyclo[2.2.1]hept-2-ene and its alkyl derivatives with cyclopentadiene in the presence of Н-form of synthetic mordenite has been studied. Phosphorus-molybdenum

Preparation method of tetracyclododecene compound

The invention discloses a preparation method of a tetracyclododecene compound. The method is characterized by comprising the following steps: mixing dicyclopentadiene, a norbornene compound and a free radical polymerization inhibitor, carrying out Diels-Alder reaction, and finally purifying to obtain the required tetracyclododecene compound, wherein the feeding molar ratio of the dicyclopentadiene to the norbornene compound is 1: (5-12). Compared with the prior art, the preparation method disclosed by the invention has the advantages that the generation of byproducts can be reduced, the effective conversion rate of dicyclopentadiene is improved, and the colorless and high-purity tetracyclododecene compound is prepared.

Preparation method and application of tetracyclic dodecene compound

The invention relates to a preparation method and application of a tetracyclic dodecene compound, the preparation method is as follows: cyclopentadiene or dicyclopentadiene is mixed with a compound shown in a formula (II), Diels-Alder addition reaction is carried out, the tetracyclic dodecene compound shown in a formula (I) is prepared, and R1 and R2 are independently selected from H or CH3. The invention provides the preparation method of the tetracyclic dodecene compound as shown in the specification, and the preparation method does not introduce any solvent, so that the energy consumption in the distillation process is reduced, and the yield of the product is increased; ethylene gas or other olefins are not used, so that the investment of equipment is reduced; meanwhile, the preparationmethod improves the conversion rate of the reaction, the obtained product is high in yield and purity, and the economy of the whole process is improved.

PREPARATION OF UNSATURATED TETRACYCLIC HYDROCARBONS AND ESTERS BASED ON THEM

Optimal conditions have been worked out for the synthesis of tetracyclo2,5.17,10.01,6>dodec-3-ene and its 8-methyl-substituted derivative by the -addition reaction of 1,3-cyclo-pentadiene to bicyclohepten