54628-90-9

Usage

Uses

Used in Pharmaceutical Industry:
3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine serves as a crucial intermediate in the synthesis of a range of drugs and pharmaceutical compounds. Its role in this industry is pivotal for the development of new medications, given its capacity to be integrated into complex molecular structures.
Used in Organic Synthesis:
In the realm of organic synthesis, 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine is utilized for its unique reactivity and structural attributes, which make it a valuable component in creating novel organic molecules with specific properties and functions.
Used in Medicinal Chemistry:
3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine also finds application in medicinal chemistry, where its structural features can be exploited to design and develop new pharmaceutical entities with improved therapeutic profiles.
Used in Biotechnology and Medical Research:
Due to potential biological activities and effects, 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine may be employed in biotechnology and medical research. Its application in these fields could lead to advancements in understanding biological processes and the development of new therapeutic strategies.

Upstream product

• 86126-32-1 1,3,3-trimethyl-6-nitro-1-(4-nitrophenyl)-2,3-dihydro-1H-indene 
• 1817-47-6 4-nitrocumene 
• 3910-35-8 1,1,3-trimethyl-3-phenylindane 
• 28094-77-1 5-chloro-3-(4-chlorophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-indene 
• 62741-13-3 2,4-bis-(4-amino-phenyl)-4-methyl-pent-2-ene 

Downstream Products

• 42499-87-6 3-(4-isocyanato-phenyl)-1,1,3-trimethyl-indan-5-yl isocyanate 

Relevant academic research and scientific papers

Method for synthesizing indane structure-containing compound

The invention provides a method for synthesizing an indane structure-containing compound, which comprises the following steps: 1) in the presence of a solid acid catalyst, carrying out a nitration reaction on an indane compound of a compound as shown in a general formula (I) to obtain compounds as shown in a general formula (II) and a general formula (III); and 2) in the presence of a reducing agent, performing a reduction reaction on the compounds represented by the general formula (II) and the general formula (III) to obtain compounds represented by the general formula (IV) and the general formula (V); wherein in the general formulas (I), (II), (III), (IV) and (V), R1, R2, R3 and R4 are independently hydrogen, C1-4 alkyl, C1-4 alkoxy, halogen, hydroxyl or carboxyl.

INDANE DERIVATIVES AND THEIR USE IN ORGANIC ELECTRONICS

The present invention relates to indane derivatives of the formula (I) and mixtures thereof, wherein X is selected from groups of the formula -A-(NAr2), wherein A is a chemical bond or phenylene which is unsubstituted or substitutedby 1, 2 or 3 substituents selected from C1-C6-alkyl and C1-C6-alkoxy; Ar is unsubstituted or substituted aryl, wherein two groups Ar bound to the same nitrogen atom may together with the nitrogen atom also form a fused ring system having 3 or more than 3 unsubstituted or substituted rings; and the variables Y, n, m, k and l are as defined in the claims and the description. The invention further relates to methods for preparing such compounds and their use in organic electronics, in particular as hole transport material or electron blocking material.