104681-54-1

Basic information

• Product Name: phenyl-3 propanedithioate de methyle
• Synonyms: phenyl-3 propanedithioate de methyle
• CAS NO: 104681-54-1
• Molecular Weight: 196.337
• Mol File: 104681-54-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl-3 propanedithioate de methyle(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl-3 propanedithioate de methyle(104681-54-1)
• EPA Substance Registry System: phenyl-3 propanedithioate de methyle(104681-54-1)

Safety Data

• Hazardous Substances Data: 104681-54-1(Hazardous Substances Data)

Upstream product

• 501-52-0 3-Phenylpropionic acid 
• 74-88-4 methyl iodide 
• 103-79-7 1-phenyl-acetone 

Downstream Products

• 126557-92-4 benzyl-2 hydroxy-3 pentanedithioate de methyle 
• 501-52-0 3-Phenylpropionic acid 
• 33148-49-1 3-phenylthiopropionic acid O-ethyl ester 
• 140869-66-5 C₂₀H₃₀N₂O₄S₂ 
• 126558-01-8 benzyl-2 oxo-3 pentanedithioate de methyle 
• 185914-06-1 methyl (E)-2-benzyl-3-(2-naphthyl)propenedithioate 
• 185914-07-2 methyl (E)-2-benzyl-3-(4-t-butylphenyl)propenedithioate 
• 185914-13-0 methyl (E)-2-benzyl-3-(4-nitrophenyl)propenedithioate 
• 185914-05-0 methyl (E)-2-benzyl-3-(4-methoxyphenyl)propenedithioate 
• 105592-27-6 benzyl-2 methyl-3 oxo-5 hexanedithioate de methyle 
• 105592-27-6 benzyl-2 methyl-3 oxo-5 hexanedithioate de methyle 
• 105592-27-6 (2S,3R)-2-Benzyl-3-methyl-5-oxo-hexanedithioic acid methyl ester 

Relevant articles and documents

ANTIFUNGAL AGENTS

Compounds of formula (I), and pharmaceutically acceptable salts thereof, may be used in therapy, for example as antifungal agents, wherein: R1, R2 and R3 are as defined herein. Certain compounds of formula (I) are also provided. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.

Substituted 1,3,4-Thiadiazoles with Anticonvulsant Activity. 2. Aminoalkyl Derivatives

This paper describes the synthesis and pharmacological evaluation of a number of substituted 1,3,4-thiadiazoles.The first member of the series, 2-(aminomethyl)-5-(2-biphenylyl)-1,3,4-thiadiazole (7) was found to possess potent anticonvulsant properties in rats and mice and compared favorably with the standard anticonvulsant drugs phenytoin, phenobarbital, and carbamazepine in a number of test situations.The potency of compound 7 was maintained on alkylation of the side-chain nitrogen atom; however, aryl substitution or chain lengthening caused a drop in potency.Replacement of the 2-biphenylyl group by phenyl or benzyl also lead to inactive compounds.