88297-77-2

Basic information

• Product Name: 1H-Inden-4-amine, 2,3-dihydro-1,1-dimethyl-
• Synonyms: 1H-Inden-4-amine,2,3-dihydro-1,1-dimethyl;1,1-dimethylindane-4-amine;4,4-dimethyl-1-aminoindan;4,4-Dimethyl-1-aminoindane;1,1-dimethyl-4-aminoindane;1,1-dimethyl-4-aminoindan;4-amino-1,1-dimethylindane
• CAS NO: 88297-77-2
• Molecular Formula: C11H15N
• Molecular Weight: 161.247
• Mol File: 88297-77-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1H-Inden-4-amine, 2,3-dihydro-1,1-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Inden-4-amine, 2,3-dihydro-1,1-dimethyl-(88297-77-2)
• EPA Substance Registry System: 1H-Inden-4-amine, 2,3-dihydro-1,1-dimethyl-(88297-77-2)

Safety Data

• Hazardous Substances Data: 88297-77-2(Hazardous Substances Data)

Usage

Derivative of indenamine

Aromatic amine

Usage

Synthesis of pharmaceuticals and organic compounds

Physical state

Clear, colorless liquid

Odor

Faint

Solubility

Soluble in organic solvents

Application

Intermediate in production of dyes, pigments, and other organic compounds

Importance

Building block in the chemical industry

Upstream product

• 74266-80-1 {2-[(2E)-1-methylbut-2-en-1-yl]phenyl}amine 

Relevant articles and documents

CYCLIZATION OF 2-(1'-ALKYL-2'-ALKENYL)ANILINES IN POLYPHOSPHORIC ACID

The cyclization of 2-alkenylarylamines in polyphosphoric acid (PPA) with 1,2 and 1,3 shifts of the α-alkyl substituent of the alkenyl fragment leads to the formation of indoline and indane compounds.Cis- and trans-stereoisomers of 2-methyl-4-ethyl-1-aminoindane formed without displacement of the α-substituents as well as 2-methyl-2-propylindoline are obtained from 2-(1'-methyl-2'-pentenyl)aniline.

CYCLIZATION OF 2-(1-METHYL-2-BUTENYL)ANILINE IN POLYPHOSPHORIC ACID

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