38997-97-6

Usage

Uses

Used in Food Industry:
1-Indan-4-yl-ethanone is used as a flavoring agent for its aromatic and sweet odor, enhancing the taste and aroma of various food products such as baked goods, confectionery, and beverages.
Used in Fragrance and Perfume Industry:
1-Indan-4-yl-ethanone is used as a fragrance ingredient in perfumes and other scented products, contributing to their pleasant and appealing aroma.
Used in Pharmaceutical Industry:
1-Indan-4-yl-ethanone is utilized in the synthesis of pharmaceuticals, serving as a key component in the development of various medicinal compounds.
Used in Cosmetic Industry:
1-Indan-4-yl-ethanone is used in cosmetic products for its aromatic properties, adding a pleasant scent to skincare, haircare, and other personal care items.

InChI:InChI=1/C11H12O/c1-8(12)10-6-2-4-9-5-3-7-11(9)10/h2,4,6H,3,5,7H2,1H3

Upstream product

• 38997-95-4 5-(tert-butyl)-2,3-dihydro-1H-indene 
• 496-11-7 INDANE 
• 75-07-0 acetaldehyde 
• 69849-04-3 2-(1-ethoxyethoxy)-2-lithiopropanenitrile 
• 38997-96-5 4-Acetyl-6-tert-butylindan 
• 917-64-6 methyl magnesium iodide 
• 15115-63-6 2,3-dihydro-1H-indene-4-carbonitrile 

Downstream Products

• 1641-41-4 4-indanol 
• 38998-04-8 7-methoxy-indan-4-ol 
• 1392286-12-2 4-(5-(2,3-dihydro-1H-inden-4-yl)-2-methyl-3-propionyl-1H-pyrrol-1-yl)benzenesulfonamide 
• 86031-42-7 4-Indancarbonsaeuremethylester 
• 4044-54-6 2,3-dihydro-1H-indene-4-carboxylic acid 

Relevant academic research and scientific papers

Annulation of aromatic imines via directed C-H bond activation

A directed C-H bond activation approach to the synthesis of indans, tetralins, dihydrofurans, dihydroindoles, and other polycyclic aromatic compounds is presented. Cyclization of aromatic ketimines and aldimines containing alkenyl groups tethered at the meta position relative to the imine directing group has been achieved using (PPh3)3RhCl (Wilkinson's catalyst). The cyclization of a range of aromatic ketimines and aldimines provides bi- and tricyclic ring systems with good regioselectivity. Different ring sizes and substitution patterns can be accessed through the coupling of monosubstituted, 1,1- or 1,2-disubstituted, and trisubstituted alkenes bearing both electron-rich and electron-deficient functionality.

Aromatic Spiranes, XXII [1]: Preparation of Cyclopenteno-4,5-indan-1-one and 2-Carbomethoxy- and 4-Chloromethyl-indane as Synthones for the Syntheses of Anellated 2,2′-Spirobiindanone

The title compounds were prepared as follows: tert.-butyl-indane (10) was formylated to give a 72:28 mixture of the aldehydes 23a and 23b which were submitted to a Knoevenagel-Doebner condensation to afford the cinnamonic acids 24. From the mixture, the p

188. Addition of Carbon Nucleophiles to Tricarbonylchromium Complexes of 1,2-Dihydrocyclobutabenzene, Indane, 1,2,3,4-Tetrahydronaphthalene and ortho-Xylene

3-Substituted 1,2-dihydrocyclobutabenzenes (bicycloocta-1,3,5-triene) are readily accessible from (1) via a two-step sequence which involves addition of a nucleophile and oxidation of the intermediate anionic

The Stereochemistry of Organometallic Compounds. XXVII. Nucleophilic and Electrophilic Substitution Reactions of Conformationally Restricted Arenechromium Compounds

The regioselectivity of reaction of tricarbonyl(1,1-dimethylindane)chromium with selected electrophiles and nucleophiles has been shown to be influenced by the preferred conformation of the tricarbonylchromium group.Nucleophiles preferentially react at carbon atoms eclipsed by a chromium-carbonyl bond and electrophiles at carbon atoms in staggered positions.When similar reactions were attempted with some chelated arenechromium dicarbonyl phosphorus compounds only low yields of substitution products were obtained.