39251-01-9

Basic information

• Product Name: S-propyl benzenecarbothioate
• Synonyms: Benzenecarbothioic acid, S-propyl ester
• CAS NO: 39251-01-9
• Molecular Formula: C₁₀H₁₂OS
• Molecular Weight: 180.2667
• Mol File: 39251-01-9.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 253.9°C at 760 mmHg
• Flash Point: 100.2°C
• Density: 1.073g/cm³
• Vapor Pressure: 0.0178mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: S-propyl benzenecarbothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-propyl benzenecarbothioate(39251-01-9)
• EPA Substance Registry System: S-propyl benzenecarbothioate(39251-01-9)

Safety Data

• Hazardous Substances Data: 39251-01-9(Hazardous Substances Data)

Upstream product

• 98-91-9 thiobenzoic acid 
• 35590-17-1 propyl benzenecarboximidoate 
• 107-03-9 1-thiopropane 
• 100-52-7 benzaldehyde 
• 611-73-4 Benzoylformic acid 
• 629-19-6 Dipropyl disulfide 
• 71-23-8 propan-1-ol 
• 65-85-0 benzoic acid 
• 98-88-4 benzoyl chloride 
• 60595-12-2 Benzaldehyd-dipropylmercaptal 
• 94-36-0 dibenzoyl peroxide 
• 13889-92-4 n-propyl chlorothioformate 
• 71-43-2 benzene 
• 98-91-9 thiobenzoic acid 

Relevant articles and documents

Poly(3,4-dimethyl-5-vinylthiazolium)/DBU-catalyzed thioesterification of aldehydes with thiols

Poly(3,4-dimethyl-5-vinylthiazolium) was synthesized from 3,4-dimethyl-5-vinylthiazole through free radical polymerization and was examined as polymer precatalysts in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) for the thioesterification of aldehydes with thiols. The poly(5-vinylthiazolium)/DBU had excellent catalytic activity and could be reused 10 times without a considerable loss of activity. To S-um up: Poly(3,4-dimethyl-5-vinylthiazolium) is examined as a polymer precatalyst in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) for the thioesterification of aldehydes with thiols. The poly(5-vinylthiazolium)/DBU system shows excellent catalytic activity and can be reused 10 times without a considerable loss of activity.

Synthesis of thioesters by simultaneous activation of carboxylic acids and alcohols using PPh3/NBS with benzyltriethylammonium tetrathiomolybdate as the sulfur transfer reagent

A new and simple route for the synthesis of thioesters starting from carboxylic acids and alcohols is reported by using tetrathiomolybdate as the key sulfur transfer reagent, Triphenylphosphane and N-bromosuccinimide were used for the activation of the ca

Convenient and efficient synthesis of thiol esters using zinc oxide as a heterogeneous and eco-friendly catalyst

A catalytic method was developed to synthesize thiol esters from the reaction of acyl chlorides and thiols using zinc oxide as a catalyst under solvent-free conditions at room temperature. Mild reaction conditions, short reaction time, excellent yields of products and recyclability of the catalyst are noteworthy features of this methodology. CSIRO 2008.