54628-90-9

Basic information

• Product Name: 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine
• Synonyms: 1H-inden-5-amine, 3-(4-aminophenyl)-2,3-dihydro-1,1,3-trimethyl-; 3-(4-Aminophenyl)-1,1,3-trimethylindan-5-amine
• CAS NO: 54628-90-9
• Molecular Formula: C₁₈H₂₂N₂
• Molecular Weight: 266.3807
• Mol File: 54628-90-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 432.3°C at 760 mmHg
• Flash Point: 257.9°C
• Density: 1.091g/cm³
• Vapor Pressure: 1.12E-07mmHg at 25°C
• Refractive Index: 1.615
• CAS DataBase Reference: 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine(54628-90-9)
• EPA Substance Registry System: 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine(54628-90-9)

Safety Data

• Hazardous Substances Data: 54628-90-9(Hazardous Substances Data)

Usage

General Description

3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine is an organic compound with the molecular formula C18H24N2. It is a tertiary amine with a substituted indane structure, containing a 4-aminophenyl functional group. 3-(4-aminophenyl)-1,1,3-trimethyl-2,3-dihydro-1H-inden-5-amine is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and pharmaceutical compounds. It may also have potential applications in the field of organic synthesis and medicinal chemistry due to its unique structure and reactivity. Additionally, it may have biological activities and effects that make it useful in biotechnology and medical research.

Upstream product

• 86126-32-1 1,3,3-trimethyl-6-nitro-1-(4-nitrophenyl)-2,3-dihydro-1H-indene 
• 62741-13-3 2,4-bis-(4-amino-phenyl)-4-methyl-pent-2-ene 
• 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 
• 1817-47-6 4-nitrocumene 

Downstream Products

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

Relevant articles and documents

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.

Electrochemical Reduction of 4-Nitroisopropylbenzene in Sulfuric Acid

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