6110-01-6

Basic information

• Product Name: 4-PHENYLSULFANYL-BUTAN-2-ONE
• Synonyms: 4-PHENYLSULFANYL-BUTAN-2-ONE;CHEMBRDG-BB 4021827;4-(phenylthio)butan-2-one(SALTDATA: FREE);4-(phenylthio)butan-2-one
• CAS NO: 6110-01-6
• Molecular Formula: C₁₀H₁₂OS
• Molecular Weight: 180.26668
• Mol File: 6110-01-6.mol
• Article Data: 71

Chemical Properties

• Boiling Point: 289 °C at 760 mmHg
• Flash Point: 140.5 °C
• Appearance: /
• Density: 1.07 g/cm³
• Vapor Pressure: 0.00227mmHg at 25°C
• Refractive Index: 1.552
• CAS DataBase Reference: 4-PHENYLSULFANYL-BUTAN-2-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-PHENYLSULFANYL-BUTAN-2-ONE(6110-01-6)
• EPA Substance Registry System: 4-PHENYLSULFANYL-BUTAN-2-ONE(6110-01-6)

Safety Data

• Hazardous Substances Data: 6110-01-6(Hazardous Substances Data)

Usage

General Description

4-PHENYLSULFANYL-BUTAN-2-ONE is a chemical compound belonging to the class of butanones. It is a colorless to pale yellow liquid with a fruity, sulfurous odor. 4-PHENYLSULFANYL-BUTAN-2-ONE is used in the synthesis of various organic compounds and is commonly employed as a starting material in the preparation of pharmaceuticals, perfumes, and flavoring agents. It is also utilized in the production of specialty chemicals and in agricultural applications. Additionally, 4-PHENYLSULFANYL-BUTAN-2-ONE is known for its potential as an intermediate in the preparation of organic materials and has been studied for its various chemical and biological properties.

InChI:InChI=1/C10H12OS/c1-9(11)7-8-12-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3

Upstream product

• 78-94-4 methyl vinyl ketone 
• 108-98-5 thiophenol 
• 6322-49-2 4-chloro-2-butanone 
• 100-68-5 methyl-phenyl-thioether 
• 69567-06-2 (N-methylanilino)prop-2-enenitrile 
• 74-88-4 methyl iodide 
• 27998-52-3 (+/-)-4-(phenylthio)-2-butanol 
• 75-09-2 dichloromethane 
• 3588-30-5 2-methoxy-1,3-butadiene 
• 882-33-7 diphenyldisulfane 
• 20524-74-7 Dibutylthioborsaeure-phenylester 

Downstream Products

• 60044-74-8 4-ethoxy-butan-2-one 
• 93766-63-3 5-Benzenesulfinyl-2-ethyl-3-hydroxy-3-methyl-pentanoic acid methyl-phenyl-amide 
• 85785-81-5 (4S,5S)-2-Methyl-2-(2-phenylsulfanyl-ethyl)-[1,3]dioxolane-4,5-dicarboxylic acid diethyl ester 
• 33944-97-7 (Z)-4-phenylsulfinyl-3-buten-2-one 
• 33944-98-8 (E)-(phenylsulfinyl)but-3-en-2-one 
• 27998-52-3 (+/-)-4-(phenylthio)-2-butanol 
• 81358-53-4 1-chloro-1-phenylthiobutan-3-one 
• 10181-99-4 4-Methylbenzo-1-thiopyrylium perchlorate 
• 108785-26-8 2-[1-Methyl-3-phenylsulfanyl-prop-(Z)-ylidene]-cyclohexanone 
• 105961-92-0 4,4-diphenylsulfenyl-2-butanone 
• 108802-24-0 (Z)-2,6-Dimethyl-8-phenylsulfanyl-oct-5-en-4-one 
• 134641-08-0 (R)-4-(phenylthio)-2-butanol 
• 110920-29-1 (S)-1-(phenylthio)-3-butanol 
• 691890-02-5 (S)-2-hydroxy-2-methyl-4-phenylthiobutyronitrile 

Relevant articles and documents

Unusual sulfanylation through ring transformation of arene-tethered 2H-pyran-2-ones by in situ built Michael adduct

A novel synthesis of highly functionalized alkylsulfanylmethyl arenes 8a-m through the ring transformation of 6-aryl-4-methyl/ethylsulfanyl-2H-pyran-2-one-3-carbonitriles 1a-j, by reaction with methyl vinyl ketone 2, is delineated and illustrated. To asce

Photo-Biocatalytic Cascades for the Synthesis of Volatile Sulfur Compounds and Chemical Building Blocks

Biocatalysis is a branch of catalysis that exploits enzymes to perform highly stereoselective chemical transformations under mild and sustainable conditions. This Synpact highlights how biocatalysis can be used in the synthesis of chiral 1,3-mercaptoalkan

Enantioselective Synthesis of Quaternary Δ4- and Δ5-Dehydroprolines Based on a Two-Step Formal [3+2] Cycloaddition of α-Aryl and α-Alkyl Isocyano(thio)acetates with Vinyl Ketones

A divergent synthesis of optically active quaternary Δ4- and Δ5-dehydro prolines is developed based on the first catalytic enantioselective conjugate addition of α-substituted isocyano(thio)acetates to vinyl ketones that is general for both α-aryl and α-alkyl isocyano(thio)acetates. The new tetrasubstituted C?N stereocenter is formed without the need of any metal salt due to a bifunctional tertiary amine/squaramide catalyst, featuring a bulky polyaryl sidearm and an unusually short squaramide diamide H???H interatomic distance in the solid state.