71057-15-3

Basic information

• Product Name: Butyric acid, 4-ethylthio-,
• Synonyms: Butyric acid, 4-ethylthio-,
• CAS NO: 71057-15-3
• Molecular Formula: C6H12 O2 S
• Molecular Weight: 148.22
• Mol File: 71057-15-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 276.7°C at 760 mmHg
• Flash Point: 121.2°C
• Appearance: /
• Density: 1.088g/cm³
• Vapor Pressure: 0.00128mmHg at 25°C
• Refractive Index: 1.49
• PKA: 4.66±0.10(Predicted)
• CAS DataBase Reference: Butyric acid, 4-ethylthio-,(CAS DataBase Reference)
• NIST Chemistry Reference: Butyric acid, 4-ethylthio-,(71057-15-3)
• EPA Substance Registry System: Butyric acid, 4-ethylthio-,(71057-15-3)

Safety Data

• Hazardous Substances Data: 71057-15-3(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron Letters, 19, p. 5211, 1978 DOI: 10.1016/S0040-4039(01)85852-4

InChI:InChI=1/C6H12O2S/c1-2-9-5-3-4-6(7)8/h2-5H2,1H3,(H,7,8)

Upstream product

• 96-48-0 4-butanolide 
• 811-51-8 sodium thioethylate 
• 83705-51-5 1-bromo-3-ethylsulfanyl-propane 
• 208593-59-3 4-ethylthiobutyric acid ethyl ester 
• 625-38-7 but-3-enoic acid 
• 75-08-1 ethanethiol 
• 4911-66-4 3-(ethylthio)propyl chloride 
• 143-33-9 sodium cyanide 

Relevant articles and documents

COMPOSITIONS, SYNTHESIS, AND METHODS OF USING PHENYLCYCLOALKYLMETHYLAMINE DERIVATIVES

The present invention provides novel phenylcycloalkylmethylamme derivatives, and methods of preparing phenylcycloalkylmethylamme derivatives. The present invention also provides methods of using phenylcycloalkylmethylamme derivatives and compositions of phenylcycloalkylmethylamme derivatives. The pharmaceutical compositions of the compounds of the present invention can be used for treating and/or preventing obesity and obesity related co- morbid indications and depression and depression related co-morbid indications.

Hard Acid and Soft Nucleophile Systems. 5. Ring-Opening Reaction of Lactones to ω-Alkylthio or ω-Arylthio Carboxylic Acids with Aluminum Halide and Thiol

Lactones were converted into ω-alkylthio carboxylic acids in high yields through ω-carbon-oxygen bond cleavage when they were treated with aluminun halide and alkanethiol.The aluminum halide and arenethiol system has also been found to be useful for the preparation of the synthetically valuable ω-arylthio carboxylic acids from lactones.