7269-35-4

Basic information

• Product Name: S-BUTYL THIOBENZOATE
• Synonyms: S-BUTYL THIOBENZOATE;N-BUTYL THIOBENZOATE;THIOBENZOIC ACID S-BUTYL ESTER;THIOBENZOIC ACID S-N-BUTYL ESTER;BUTYL THIOBENZOATE;Thiobenzoicacidbutylester;S-Butyl Thiobenzoate,Thiobenzoic Acid S-Butyl Ester;S-Butyl Thiobenzoate
• CAS NO: 7269-35-4
• Molecular Formula: C₁₁H₁₄OS
• Molecular Weight: 194.29
• Mol File: 7269-35-4.mol
• Article Data: 32

Chemical Properties

• Melting Point: 119 °C
• Boiling Point: 160 °C / 23mmHg
• Appearance: /
• Density: 1,05 g/cm3
• Refractive Index: 1.5520-1.5550
• CAS DataBase Reference: S-BUTYL THIOBENZOATE(CAS DataBase Reference)
• NIST Chemistry Reference: S-BUTYL THIOBENZOATE(7269-35-4)
• EPA Substance Registry System: S-BUTYL THIOBENZOATE(7269-35-4)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 7269-35-4(Hazardous Substances Data)

Usage

General Description

S-Butyl thiobenzoate is a chemical compound that belongs to the thioester group. It is a clear, colorless to pale yellow liquid with a characteristic odor and is commonly used as a flavoring agent in the food and beverage industry. S-Butyl thiobenzoate is also utilized as a fragrance ingredient in cosmetics and personal care products. It is known for its strong odor and is often used to add a garlic-like note to various products. Additionally, this chemical compound is widely used as a solvent in industrial and manufacturing processes. Overall, S-Butyl thiobenzoate is a versatile compound with a wide range of applications in different industries.

Upstream product

• 109-79-5 n-butanethiol 
• 98-88-4 benzoyl chloride 
• 629-45-8 dibutyl disulfide 
• 613-94-5 benzoic acid hydrazide 
• 2386-60-9 perfluoro-1-butanesulfonyl fluoride 
• 13939-06-5 molybdenum hexacarbonyl 
• 98-80-6 phenylboronic acid 
• 1112-67-0 tetrabutyl-ammonium chloride 
• 65-85-0 benzoic acid 
• 1643-19-2 tetrabutylammomium bromide 
• 311-28-4 tetra-(n-butyl)ammonium iodide 
• 109-65-9 1-bromo-butane 
• 93-97-0 benzoic acid anhydride 
• 201230-82-2 carbon monoxide 

Downstream Products

• 29526-96-3 1-phenylcyclopropan-1-ol 
• 455-32-3 benzoyl fluoride 
• 1336932-04-7 (E)-3-butylthio-1-phenyl-2-undecen-1-one 
• 1336932-05-8 (Z)-3-butylthio-1-phenyl-2-undecen-1-one 
• 20129-23-1 butyl phenyl disulfide 
• 884-09-3 phenyl thiobenzoate 
• 136-60-7 benzoic acid, butyl ester 
• 35822-90-3 benzoyl-tert-butylnitroxyl radical 
• 58921-68-9 N-tert-butyl-N-n-butylthio nitroxide radical 
• 77839-05-5 C₁₉H₃₂NO₂S₂ 
• 6744-67-8 C₁₁H₁₄O₄S 
• 2386-47-2 butane-1-sulfonic acid 

Relevant articles and documents

Preparation method of thioester compounds

The invention discloses a preparation method of thioester compounds, wherein the method comprises the following steps: adding nickel trifluoromethanesulfonate, 4,4'-di-tert-butyl-2,2'-dipyridyl, carbonyl molybdenum, potassium carbonate, zinc iodide, water

Synthesis of selenol esters via the reaction of acyl chlorides with diselenides in the presence of Zn dust catalyzed by CoCl2·6H2O

A practical and efficient approach for the synthesis of selenol and thiol esters is described via the reaction of acyl chlorides with diselenides or disulfides in the presence of Zn dust catalyzed by inexpensive CoCl2·6H2O This proto

Nickel-Catalyzed Thiocarbonylation of Arylboronic Acids with Sulfonyl Chlorides for the Synthesis of Thioesters

An interesting procedure for thioester synthesis via nickel-catalyzed thiocarbonylation of arylboronic acid with sulfonyl chlorides as the sulfur source has been explored. Using Mo(CO)6 as a solid CO surrogate and reductant, a broad range of thioesters were obtained in moderate to good yields with good functional group tolerance.