2018-87-3

Usage

Uses

Used in Pharmaceutical Synthesis:
2,3-dibromotetralin is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Production:
In the agrochemical industry, 2,3-dibromotetralin is used as a starting material for the production of various agrochemicals. Its properties contribute to the development of effective compounds for agricultural use.
Used in Fragrance Industry:
2,3-dibromotetralin is used as a component in the creation of fragrances. Its chemical structure lends itself to the development of unique and complex scents for use in perfumes and other scented products.
Used in Organic Compound Preparation:
2,3-dibromotetralin serves as an important intermediate in the preparation of other organic compounds. Its versatility in chemical reactions makes it a valuable asset in the synthesis of a wide range of chemical products.
Used in Biological Research:
Due to its potential antioxidant and antitumor properties, 2,3-dibromotetralin is used in biological research to study its effects on various biological systems and to explore its potential as a therapeutic agent.

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 447-53-0 1,2-Dihydronaphthalene 
• 634-36-6 1,2,3-trimethoxybenzene 

Downstream Products

• 447-53-0 1,2-Dihydronaphthalene 
• 14211-53-1 cis-1,2-dihydroxy-1,2,3,4-tetrahydronaphthalene 
• 14211-53-1 trans-naphthalene-1,2,3,4-tetrahydro-1,2-diol 
• 91-20-3 naphthalene 
• 119-64-2 tetralin 
• 612-94-2 2-phenylnaphthalene 
• 7480-36-6 (+/-)-trans-1-amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene 
• 86800-08-0 trans-N-Benzyl-α-amino-β-tetralol 
• 530-91-6 1,2,3,4-tetrahydronaphthalen-2 ol 
• 1056246-70-8 2-bromo-1-tetralone 
• 78407-08-6 1-Methylamino-1,2,3,4-tetrahydro-[2]naphthol 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 92013-27-9 3-bromo-1,2-dihydroxynaphthalene 

Relevant academic research and scientific papers

Samarium triflate-catalyzed halogen-promoted Friedel-Crafts alkylation with alkenes

A versatile and efficient halogen-promoted highly regio- and stereoselective Friedel - Crafts (F-C) alkylation with alkenes has been developed with use of easily available and inexpensive NBS or I2 as the efficient halogen sources. Lewis acids, in particular metal triflates, are found to be effective catalysts for this halogen-promoted F-C alkylation. Among these, Sm(OTf)3 was the best catalyst. Electron-rich arenes smoothly underwent F-C alkylation with a variety of alkenes including α,β-unsaturated carbonyl compounds.