3260-63-7

Usage

Uses

Used in Perfumery Industry:
N-METHYLINDOXYL ACETATE is used as a perfume ingredient for its strong, floral odor, contributing to the creation of various fragrances.
Used in Flavor and Fragrance Industry:
N-METHYLINDOXYL ACETATE is used as a flavoring agent for its sweet and floral taste, enhancing the taste profiles of food products.
Used in Cosmetics Industry:
N-METHYLINDOXYL ACETATE is used in the formulation of scents for cosmetics, adding a pleasant floral aroma to products such as body lotions, soaps, and shampoos.
Used in Food and Beverage Industry:
N-METHYLINDOXYL ACETATE is used as a flavor enhancer in food and beverage products, providing a sweet and floral taste to a variety of items.

InChI:InChI=1/C11H11NO2/c1-8(13)14-11-7-12(2)10-6-4-3-5-9(10)11/h3-7H,1-2H3

Upstream product

• 119-68-6 N-Methylanthranilic acid 
• 21716-67-6 2-(carboxymethyl)-N-methylanthranilic acid 
• 108-24-7 acetic anhydride 
• 120-72-9 indole 
• 603-76-9 1-methylindole 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 618-40-6 1-Methyl-1-phenylhydrazine 
• 213339-77-6 1-methyl-2-(triisopropylsilyl)-1H-indole 

Downstream Products

• 38072-62-7 2-(4-Chlorphenyl)-methyliden-1-methylindolin-3-on 
• 38072-61-6 2-(4-Chlorphenyl)-methyliden-1-methylindolin-3-on 
• 38072-58-1 (E)-2-benzylidene-1-methylindolin-3-one 
• 38072-57-0 (Z)-2-benzylidene-1-methylindolin-3-one 
• 84584-97-4 (E/Z)-2-benzylidene-1-methylindolin-3-one 
• 84353-53-7 2-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-1-methyl-1,2-dihydro-indol-3-one 
• 84353-53-7 2-[1-(4-Methoxy-phenyl)-meth-(Z)-ylidene]-1-methyl-1,2-dihydro-indol-3-one 
• 99430-49-6 3-hydroxy-1-methylindole-2-carbaldehyde 
• 99430-58-7 3-Oxo-1-methyl-2-(N-methyl-N-phenylaminomethylene)indole 
• 125141-07-3 1-Methyl-2-[1-phenylamino-eth-(E)-ylidene]-1,2-dihydro-indol-3-one 
• 125141-08-4 1-Methyl-2-[1-p-tolylamino-eth-(E)-ylidene]-1,2-dihydro-indol-3-one 
• 125141-11-9 2-[1-Benzylamino-eth-(E)-ylidene]-1-methyl-1,2-dihydro-indol-3-one 
• 125141-09-5 2-[1-(4-Methoxy-phenylamino)-eth-(E)-ylidene]-1-methyl-1,2-dihydro-indol-3-one 
• 125141-10-8 4-{1-[1-Methyl-3-oxo-1,3-dihydro-indol-(2E)-ylidene]-ethylamino}-benzoic acid methyl ester 

Relevant academic research and scientific papers

Co(III)-Catalyzed, Internal and Terminal Alkyne-Compatible Synthesis of Indoles

A Co(III)-catalyzed, internal and terminal alkyne-compatible indole synthesis protocol is reported herein. The N-amino (hydrazine) group imparts distinct, diverse reactivity patterns for directed C-H functionalization/cyclization reactions. Notable synthetic features include regioselectivity for a meta-substituted arylhydrazine, regioselectivity for a chain-branched terminal alkyne, formal incorporation of an acetylenic unit through C2-desilylation on a C2-silylated indole derivative, formal inversion of regioselectivity through consecutive C3-derivatization and C2-desilylation processes, and formal bond migration for a linear-chain terminal alkyne.

Copper-catalysed direct C-H bond oxidative acetoxylation and iodination of indoles

A novel Cu(OAc)2-catalysed direct C-H bond oxidative acetoxylation and iodination of indoles using PhI(OAc)2 as a terminal oxidant is reported. Adopting this method, a series of 3-iodoindoles and indol-3-yl acetates were obtained in nearly 1:1 ratio yield.

Pd-catalyzed direct and selective C-H functionalization: C3-acetoxylation of indoles

Direct functionalization of C-H bonds has been a hot topic in organic chemistry during recent years. Arenes-one of the most abundant chemical motifs-usually have multiple C-H bonds. Although, some examples of direct functionalizations of arenes have been