33982-85-3

Basic information

• Product Name: Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)- (9CI)
• Synonyms: Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)- (9CI);1-Indan-2-yl-ethanone;Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)-
• CAS NO: 33982-85-3
• Molecular Formula: C₁₁H₁₂O
• Molecular Weight: 160.21238
• Product Categories: ACETYLGROUP
• Mol File: 33982-85-3.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)- (9CI)(33982-85-3)
• EPA Substance Registry System: Ethanone, 1-(2,3-dihydro-1H-inden-2-yl)- (9CI)(33982-85-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 33982-85-3(Hazardous Substances Data)

Usage

Uses

1-Indan-2-yl-ethanone is used in the synthetic preparation of benzocycloalkene derivatives as agricultural fungicides as well as chemo- and diastereoselective preparations of cyclic endoperoxides by potassium hydroxide-mediated three-component cyclization reactions.

Upstream product

• 54454-67-0 1-Indan-2-yl-2-(triphenyl-λ⁵-phosphanylidene)-ethanone 
• 1575-74-2 (+-)-2-methyl-pent-4-enoic acid 
• 71-43-2 benzene 
• 91-13-4 α,α'-dibromo-o-xylene 
• 123-54-6 acetylacetone 
• 86737-24-8 ethyl 2-acetyl-2,3-dihydro-1H-indene-2-carboxylate 
• 615-13-4 2-indanone 
• 54454-41-0 Triphenyl-{2-[2-(triphenyl-λ⁵-phosphanylidene)-acetyl]-indan-2-yl}-phosphonium; bromide 
• 544-97-8 dimethyl zinc(II) 

Downstream Products

• 1315590-37-4 SRC 689 
• 1315590-39-6 C₂₃H₂₅F₃O₃ 
• 1401619-05-3 1-(1-(4-chlorobenzyl)-1H-indole-2-carbonyl)-N-(1-(2,3-dihydro-1H-inden-2-yl)ethyl)piperidine-4-carboxamide 

Relevant articles and documents

A concise synthesis of atipamezole

Atipamezole (1), a potent α2 adrenergic receptor antagonist, was synthesized in four steps from dibromide 2 and 2,4-pentanedione.

An unexpected directing effect in the asymmetric transfer hydrogenation of α,α-disubstituted ketones

α,α-Disubstituted ketones containing an aromatic ring or alkene are reduced in high enantiomeric excess using an asymmetric transfer hydrogenation catalyst. The sense of reduction indicates that the unsaturated region of the ketone adopts a position adjacent to the Ru-bound η6-arene ring in the reduction transition state.