94568-76-0

Basic information

• Product Name: 1,1,3-Trimethyl-2,3-dihydro-1H-inden-4-amine
• Synonyms: 1,1,3-Trimethyl-2,3-dihydro-1H-inden-4-amine;1,1,3-Trimethyl-indan-4-ylamine
• CAS NO: 94568-76-0
• Molecular Formula: C12H17N
• Molecular Weight: 175.27008
• Mol File: 94568-76-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 264.4℃ at 101.33kPa
• Appearance: /
• Density: 0.98 at 20℃
• Vapor Pressure: 0.2-0.39Pa at 20-25℃
• CAS DataBase Reference: 1,1,3-Trimethyl-2,3-dihydro-1H-inden-4-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,3-Trimethyl-2,3-dihydro-1H-inden-4-amine(94568-76-0)
• EPA Substance Registry System: 1,1,3-Trimethyl-2,3-dihydro-1H-inden-4-amine(94568-76-0)

Safety Data

• Hazardous Substances Data: 94568-76-0(Hazardous Substances Data)

Usage

Uses

4-Amino-1,1,3-trimethylindane is used as a reagent in the synthesis of (difluoromethylnicotinic)indanyl carboxamides as fungicides useful in crop protection.

Upstream product

• 4497-58-9 1,2,3,4-tetrahydro-2,2,4-trimethylquinoline 
• 4497-59-0 1-acetyl-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline 
• 5855-23-2 1-(2,2,4-trimethylquinolin-1(2H)-yl)ethan-1-one 
• 147-47-7 2,2,4-trimethyl-1,2-dihydroquinoline 
• 4325-82-0 4-methyl pent-3-en-2-ol 
• 62-53-3 aniline 
• 746625-44-5 2-(1,3-dimethylbut-2-enyl)aniline 
• 125349-37-3 (3R)-1,1,3-trimethyl-4-aminoindane 

Downstream Products

• 1246263-35-3 2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide 
• 1616291-21-4 4-amino-1,1,3-trimethylindane hydrochloride 

Relevant articles and documents

PROCESS FOR PRODUCING SUBSTITUTED 4-AMINOINDANES

The present invention primarily relates to a process for producing certain substituted 2-allylanilines of the hereinbelow-defined formula (I) and their use in a process for producing substituted 4-aminoindane derivatives of the hereinbelow-defined formula

METHOD FOR PRODUCING RACEMATE OF COMPOUND

A method for producing a racemate of a compound represented by Formula (1), including bringing a transition metal catalyst into contact with an optically active form of the compound represented by Formula (1): [in Formula (1), a ring X1 represents an aromatic ring; R1 represents a C1-6 alkyl group, a C3-8 cycloalkyl group, or a C1-6 halo-alkyl group; R2 is a group different from R1 and represents a C1-6 alkyl group, a C3-8 cycloalkyl group, or a C1-6 halo-alkyl group, or R2 and the ring X1 are bonded to each other to form a ring; a hydrogen atom(s) of the ring X1 is optionally replaced with a C1-6 alkyl group, a C1-6 halo-alkyl group, a cyano group, a nitro group, a C1-6 alkoxy group, or a halogen atom; and * represents an asymmetric carbon atom].

BENZAMIDIC COMPOUNDS HAVING FUNGICIDAL ACTIVITY AND RELATIVE USE

The present invention relates to benzamidic compounds having general formula (I): wherein: Rx represents a halogen atom or a methyl group possibly substituted by fluorine atoms; R1, R2, R3, independently from each other, represent a C1- C3 alkyl group; R4 represents a hydrogen atom or a C1-C3 alkyl group; Ry represents a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alcoxy group, a C1-C4 haloalcoxy group; n represents an integer ranging of from 0 to 3. The present invention also relates to the use of the above benzamidic compounds for the control of fungi, bacteria and phytopathogenic viruses of agricultural crops.