65001-59-4

Basic information

• Product Name: 2,5,7-TRIMETHYL-INDAN-1-ONE
• Synonyms: 2,5,7-TRIMETHYL-INDAN-1-ONE;2,3-Dihydro-2,5,7-trimethyl-1H-inden-1-one;2,5,7-TriMethyl-2,3-dihydro-1H-inden-1-one
• CAS NO: 65001-59-4
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.23896
• Mol File: 65001-59-4.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 294℃
• Flash Point: 124℃
• Appearance: /
• Density: 1.039
• Vapor Pressure: 0.002mmHg at 25°C
• Refractive Index: 1.544
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,5,7-TRIMETHYL-INDAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5,7-TRIMETHYL-INDAN-1-ONE(65001-59-4)
• EPA Substance Registry System: 2,5,7-TRIMETHYL-INDAN-1-ONE(65001-59-4)

Safety Data

• Hazardous Substances Data: 65001-59-4(Hazardous Substances Data)

Usage

General Description

2,5,7-Trimethyl-indan-1-one is a chemical compound with the molecular formula C13H16O. It is a bicyclic ketone containing a seven-membered ring, and it is characterized by its strong, sweet, woody odor. 2,5,7-TRIMETHYL-INDAN-1-ONE is often used in the fragrance industry as a key component in various perfumes and aromatic products. It has also been studied for its potential therapeutic applications, including its ability to act as an inhibitor of acetylcholinesterase, an enzyme involved in the breakdown of the neurotransmitter acetylcholine. Furthermore, 2,5,7-Trimethyl-indan-1-one has also been investigated for its antimicrobial and antioxidant properties, making it a versatile and valuable compound in both the fragrance and pharmaceutical industries.

InChI:InChI=1/C12H14O/c1-7-4-8(2)11-10(5-7)6-9(3)12(11)13/h4-5,9H,6H2,1-3H3

Upstream product

• 65001-58-3 3-(3,5-Dimethylphenyl)-2-methyl-2-propensaeureethylester 
• 23351-72-6 1-isobutyryl-2,4-dimethylbenzene 
• 52528-74-2 Diethyl(3,5-dimethylphenylmethyl)methylmalonate 
• 27129-86-8 1-bromomethyl-3,5-dimethylbenzene 
• 108-67-8 1,3,5-trimethyl-benzene 
• 618084-17-6 5-(3,5-dimethylbenzyl)-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 5779-95-3 3,5-dimethylbenzaldehyde 
• 848610-64-0 5-(3,5-dimethylbenzyl)-2,2,5-trimethyl-1,3-dioxane-4,6-dione 
• 97-63-2 methyl methacrylate 
• 108-38-3 m-xylene 
• 61227-50-7 β-(3,5-dimethylphenyl)-α-methylpropionic acid 
• 105902-38-3 2-bromo-1-(2,4-dimethylphenyl)-2-methylpropan-1-one 

Downstream Products

• 150096-40-5 2,4,6-trimethyl-indene 
• 95-13-6 1-indene 

Relevant articles and documents

Synthesizing method of indanone compound

The invention discloses a synthesizing method of an indanone compound. The synthesizing method comprises the following steps of respectively adding a catalyst and an antioxidant into a reaction bottle, then adding a compound shown in a formula (2), adding a solvent, and reacting for 2 to 6h at the temperature of 70 to 120 DEG C under the argon protection atmosphere, so as to obtain the indanone compound, wherein the catalyst is selected from any one of Cu(OAc)2, CuCl2 (copper (II) chloride), CuBr2 (copper (II) bromide), CuO (copper oxide), CuF2 (copper fluoride), Cu(OTf) 2, Cu(OH)2 (copper hydroxide), Cu(NO3)2 (copper nitrate), CuCl (copper chloride), CuBr (copper bromide), CuI (cuprous iodide) and Cu2O (cuprous oxide); the oxidant is tert-butyl hydroperoxide; the solvent is toluene. The synthesizing method has the advantages that a novel concept of the indanone compound is provided; the copper catalyst is used, the price of copper is low, the reserve amount is rich, the environment-friendly effect is realized, and the hydroacylation reaction catalyzed by copper meets the requirements of green chemistry.

A method of preparation of ethylene-propylene-diene rubber

The invention discloses a bridged metallocene complex, which is characterized by having a structural formula shown as the following A1, A2, A3 or A4. The invention also discloses a preparation method of ethylene propylene rubber. The ethylene propylene ru

Catalytic intramolecular friedel-crafts reaction of benzyl meldrum's acid derivatives: Preparation of 5,6-dimethoxy-2-methyl-1-indanone

-