58443-71-3

Basic information

• Product Name: S-PHENYL THIOISOBUTYRATE)
• Synonyms: S-PHENYL THIOISOBUTYRATE)
• CAS NO: 58443-71-3
• Molecular Formula: C₁₀H₁₂OS
• Molecular Weight: 180.26668
• Mol File: 58443-71-3.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 260.73°C at 760 mmHg
• Flash Point: 104.591°C
• Appearance: /
• Density: 1.056 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.012mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: S-PHENYL THIOISOBUTYRATE)(CAS DataBase Reference)
• NIST Chemistry Reference: S-PHENYL THIOISOBUTYRATE)(58443-71-3)
• EPA Substance Registry System: S-PHENYL THIOISOBUTYRATE)(58443-71-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39
• Hazardous Substances Data: 58443-71-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H12OS/c1-8(2)10(11)12-9-6-4-3-5-7-9/h3-8H,1-2H3

Upstream product

• 108-98-5 thiophenol 
• 79-31-2 isobutyric Acid 
• 201230-82-2 carbon monoxide 
• 882-33-7 diphenyldisulfane 
• 78-84-2 isobutyraldehyde 
• 83078-46-0 2-Methyl-dithiopropionsaeure-phenylester 
• 981-18-0 triphenyl(phenylazo)methane 
• 1192-40-1 copper(I) thiophenolate 
• 79-30-1 isobutyryl chloride 
• 930-69-8 sodium thiophenolate 
• 2973-86-6 lithium thiophenoxide 
• 178943-91-4 isobutyryl 2,4,6-trichlorobenzoyl anhydride 
• 13464-19-2 phenyl chlorothioformate 
• 1068-55-9 isopropylmagnesium chloride 

Downstream Products

• 52411-62-8 phenyl 3-hydroxy-2,2-dimethyl-3-phenylpropanethioate 
• 183050-86-4 C₆H₅S₄^(1-) 
• 174576-52-4 (R)-4-((S)-1-Benzyloxy-ethyl)-3,3-dimethyl-oxetan-2-one 
• 83078-46-0 2-Methyl-dithiopropionsaeure-phenylester 
• 611-70-1 phenyl isopropyl ketone 
• 5463-82-1 2-methyl-3-decanone 
• 131436-04-9 4-(2-phenylethyl)-3,3,4-trimethyloxetan-2-one 
• 15621-60-0 isobutyryl-coenzyme A 
• 7570-96-9 2-naphthyl phenyl sulfide 
• 66928-65-2 (3,4-dimethylpent-3-en-1-yl)benzene 
• 54934-28-0 S-phenyl 2,2-dimethyl-3-oxo-3-phenylpropanethioate 

Relevant articles and documents

Compound embodiments that release H2S by reaction with a reactive compound and methods of making and using the same

Disclosed herein are embodiments of a donor compound that releases H2S by reacting with a reactive compound. The donor compound embodiments described herein can be used to deliver H2S to a subject or a sample and further can be used to administer therapeutic agents. The donor compound embodiments also can facilitate bioconjugation. Methods of making and using the donor compound embodiments also are disclosed.

Manganese(iii)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters

A Mn(iii)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yieldsviaradical intermediates.

Beta-lactones as antibacterial agents

The present invention relates to specific beta-lactone compounds and compositions thereof for the treatment of infections, such as, e.g., infections with bacteria or infections with protozoa, in particular infections with Gram-positive and/or Gram-negativ