15972-15-3

Basic information

• Product Name: 1,3-Butanedione, 1-cyclohexyl-
• CAS NO: 15972-15-3
• Molecular Formula: C10H16O2
• Molecular Weight: 168.236
• Mol File: 15972-15-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,3-Butanedione, 1-cyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Butanedione, 1-cyclohexyl-(15972-15-3)
• EPA Substance Registry System: 1,3-Butanedione, 1-cyclohexyl-(15972-15-3)

Safety Data

• Hazardous Substances Data: 15972-15-3(Hazardous Substances Data)

Usage

General Description

1,3-Butanedione, 1-cyclohexyl-, commonly known as cyclohexyl methyl ketone, is a chemical compound that is used primarily as a flavoring agent in the food and beverage industry. It is a clear, colorless liquid with a sweet, creamy odor and is often used to add a buttery flavor to various food products. It is also used in the production of perfumes and as a solvent in some industrial processes. However, it is important to note that exposure to high levels of this chemical can be harmful, causing irritation to the eyes, skin, and respiratory tract, as well as potential systemic toxicity. Therefore, strict safety guidelines and regulations are in place for its use and handling in various industries.

Upstream product

• 79-20-9 acetic acid methyl ester 
• 823-76-7 Cyclohexyl methyl ketone 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 797752-46-6 4-cyclohexyl-4-hydroxy-1-phenylsulfonyl-2-butanone 
• 67-64-1 acetone 
• 141-78-6 ethyl acetate 
• 141-52-6 sodium ethanolate 

Downstream Products

• 40601-43-2 diethyl (2-cyclohexyl-2-oxoethyl)phosphonate 
• 1610378-75-0 C₁₄H₂₄O₃ 
• 91481-29-7 (4-Amino-2-methyl-5-phenyl-1H-pyrrol-3-yl)-cyclohexyl-methanone; hydrochloride 
• 948855-98-9 4-amino-6-cyclohexyl-5-(1-hydroxyethyl)-2-methylpyridazin-3(2H)-one 
• 948855-96-7 5-acetyl-4-amino-6-cyclohexyl-2-methylpyridazin-3(2H)-one 
• 948855-95-6 4-cyclohexyl-3,6-dimethylisoxazolo[3,4-d]pyridazin-7(6H)-one 
• 948855-94-5 4-cyclohexanecarbonyl-5-methylisoxazole-3-carboxylic acid ethyl ester 
• 3289-28-9 ethyl cyclohexanecarboxylate 
• 141-78-6 ethyl acetate 
• 823-76-7 Cyclohexyl methyl ketone 
• 67-64-1 acetone 

Relevant articles and documents

Pyrrolecarboxylic acid derivative synthesis method

The invention discloses a pyrrolecarboxylic acid derivative synthesis method, which comprises: obtaining a group substituted formylacetone derivative by using a group substituted acetyl derivative andethyl acetate as raw materials; carrying out cyclization with diethyl aminomalonate hydrochloride to generate a pyrrolecarboxylic acid derivative ethyl ester; and carrying out a hydrolysis reaction to obtain the target product pyrrolecarboxylic acid derivative. According to the present invention, the method has characteristics of mild reaction conditions, simple purification, high yield and highproduct purity, and is suitable for process amplification and mass production.

Enantioselective cascade formal reductive insertion of allylic alcohols into the C(O)-C bond of 1,3-diketones: Ready access to synthetically valuable 3-alkylpentanol units

An unprecedented cascade reaction combining dual iron-amine-catalyzed enantioselective functionalization of allylic alcohols and chemoselective acyl transfer is presented. It allows, from diketones and allylic alcohols, preparation of efficiently function

Synthesis and pharmacological evaluation of a series of analgesic and antiinflammatory 4-aminopyrroles

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