1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine

Base Information

• Chemical Name: 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine
• CAS No.: 94568-76-0
• Molecular Formula: C12H17N
• Molecular Weight: 175.27000
• European Community (EC) Number: 838-724-1
• Mol file: 94568-76-0.mol

Synonyms:1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine;94568-76-0;4-amino-1,1,3-trimethylindane;1,1,3-Trimethyl-indan-4-ylamine;1,1,3-trimethyl-2,3-dihydroinden-4-amine;1H-Inden-4-amine, 2,3-dihydro-1,1,3-trimethyl-;SCHEMBL2779868;1,1,3-Trimethyl-4-aminoindan;1,1,3-trimethyl-4-aminoindane;1,1,3-trimethylindane-4-amine;KYWYAWFSWFSPAY-UHFFFAOYSA-N;MFCD20691224;SB40149;racemic 1,1,3-trimethyl-4-aminoindane;AS-48056;EN300-393223;F17604

Chemical Property of 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine

Chemical Property:

• Vapor Pressure: 0.2-0.39Pa at 20-25℃
• Boiling Point: 264.4℃ at 101.33kPa
• PSA: 26.02000
• Density: 0.98 at 20℃
• LogP: 3.63480
• XLogP3: 3.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 175.136099547
• Heavy Atom Count: 13
• Complexity: 197

Purity/Quality:

99.9% ^*data from raw suppliers

4-Amino-1,1,3-trimethylindane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1CC(C2=C1C(=CC=C2)N)(C)C
• 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.

Technology Process of 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine

There total 8 articles about 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

1-acetyl-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline (4497-59-0) → 4-amino-1,1,3-trimethylindane (94568-76-0)

Guidance literature:

1-acetyl-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline; With hydrogen fluoride; at 0 - 19 ℃; for 20h;

With water; at 100 ℃; for 6h;

Reference yield: 69.0%

→ 4-amino-1,1,3-trimethylindane (94568-76-0)

Guidance literature:

Reference yield:

2-(1,3-dimethylbut-2-enyl)aniline (746625-44-5) → 4-amino-1,1,3-trimethylindane (94568-76-0)

Guidance literature:

With sulfuric acid; In water; at 5 - 22 ℃; for 4h;

upstream raw materials:

1,2,3,4-tetrahydro-2,2,4-trimethylquinoline

1-acetyl-2,2,4-trimethyl-1,2,3,4-tetrahydroquinoline

1-(2,2,4-trimethylquinolin-1(2H)-yl)ethan-1-one

2,2,4-trimethyl-1,2-dihydroquinoline

Downstream raw materials:

2-fluoro-6-(trifluoromethyl)-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)benzamide

4-amino-1,1,3-trimethylindane hydrochloride

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