16696-68-7

Basic information

• Product Name: 1-phenylethanethione
• Synonyms: Ethanethione, 1-phenyl-
• CAS NO: 16696-68-7
• Molecular Formula: C₈H₈S
• Molecular Weight: 136.2141
• Mol File: 16696-68-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 201.7°C at 760 mmHg
• Flash Point: 75.8°C
• Density: 1.057g/cm³
• Vapor Pressure: 0.431mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 1-phenylethanethione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenylethanethione(16696-68-7)
• EPA Substance Registry System: 1-phenylethanethione(16696-68-7)

Safety Data

• Hazardous Substances Data: 16696-68-7(Hazardous Substances Data)

Upstream product

• 507-09-5 thioacetic acid 
• 1749-19-5 phenyl(1-phenylethylidene)amine 
• 7647-01-0 hydrogenchloride 
• 7740-33-2 ethyl 3-thioxobutanoate 
• 64-17-5 ethanol 
• 98-86-2 acetophenone 
• 60-29-7 diethyl ether 
• 33877-11-1 1-Phenylethanethiol 
• 4556-23-4 pyridine-4-thiol 
• 99-91-2 para-chloroacetophenone 
• 838-59-5 bis-(1-phenyl-ethyl)-sulfide 
• 23181-78-4 2,4-Dimethyl-2,4,6-triphenyl-4H-[1,3]dithiin 
• 84065-89-4 2-Methyl-2-phenyl-1,3-dithiolan-1,1-dioxid 
• 512-22-1 2,4,6-trimethyl-2,4,6-triphenyl-[1,3,5]trithiane 

Downstream Products

• 512-22-1 2,4,6-trimethyl-2,4,6-triphenyl-[1,3,5]trithiane 
• 62241-66-1 3exo,5,6-trimethyl-3endo,7-diphenyl-2-thia-7-phospha-bicyclo[2.2.1]hept-5-ene 7syn-sulfide 
• 100-42-5 styrene 
• 100-41-4 ethylbenzene 
• 7783-06-4 hydrogen sulfide 
• 98-86-2 acetophenone 
• 873-32-5 2-Chlorobenzonitrile 
• 133113-59-4 3-(2-Chloro-phenyl)-5-methyl-5-phenyl-[1,4,2]dithiazole 
• 117053-98-2 3-(4-Methoxy-phenyl)-5-methyl-5-phenyl-[1,4,2]dithiazole 
• 874-90-8 4-methoxybenzonitrile 
• 117053-97-1 5-Methyl-3-(4-nitro-phenyl)-5-phenyl-[1,4,2]dithiazole 
• 619-72-7 4-nitrobenzonitrile 
• 3328-86-7 2,4-diphenylthiophene 
• 98203-29-3 2,5-bis<(diphenylmethylene)amino>thiophene-3,4-dicarbonitrile 

Relevant articles and documents

Reactions of 1,3-Epithionaphtho5,6λ5>thiadiphosphinine-1,3-dithione; the Preparation and X-ray Structure of NpP(S)(SMe)SP(S)(OMe), the first C3P2S Ring

NpP2S4 1 (Np = C10H6, naphthalene-1,8-diyl) reacts with carbonyl groups to give thiocarbonyls whilst refluxing 1 in methanol results in cleavage of one of the P-S-P bridges and formation of the new heterocycle 3 which contains a C3P2S ring with the phosph

Stereospecific Reactions of Donor–Acceptor Cyclopropanes with Thioketones: Access to Highly Substituted Tetrahydrothiophenes

Lewis-acid-catalyzed reactions of 2-substituted cyclopropane 1,1-dicarboxylates with thioketones are described. Highly substituted tetrahydrothiophenes with two adjacent quaternary carbon atoms were obtained in a stereospecific manner under mild conditions and in high yield when using AlCl3 as Lewis acid. Moreover, an intramolecular approach was successfully implemented to gain access to sulfur-bridged [n.2.1] bicyclic ring systems. Conversion of selenoketones, the heavier analogues, under similar conditions resulted in the formation of various tetrahydroselenophenes.

METHODS FOR TREATING OR PREVENTING AN INFLAMMATORY OR METABOLIC CONDITION OR INHIBITING JNK

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