101093-83-8

Basic information

• Product Name: Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]-
• CAS NO: 101093-83-8
• Molecular Formula: C15H14O3S
• Molecular Weight: 274.34
• Mol File: 101093-83-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]-(101093-83-8)
• EPA Substance Registry System: Benzoic acid, 2-[[(4-methoxyphenyl)methyl]thio]-(101093-83-8)

Safety Data

• Hazardous Substances Data: 101093-83-8(Hazardous Substances Data)

Upstream product

• 2746-25-0 p-Methoxybenzyl bromide 
• 147-93-3 Thiosalicylic acid 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1183312-78-8 2-(4-methoxy-benzylsulfinyl)-benzoic acid 
• 54705-26-9 ortho-[(N-methyl)carbamoyl]phenyl benzyl sulfoxide 
• 95971-74-7 N-(1-phenylbutyl)acetamide 
• 20054-45-9 N-methyl-2-sulfanylbenzamide 
• 2884-02-8 4-methyl-1-phenyl-pentan-1-ol 
• 54705-19-0 2-(benzylthio)-N-methylbenzamide 
• 144121-60-8 1-phenylhex-5-en-1-ol 
• 30078-89-8 1,4-diphenyl-1-butanol 
• 1315275-25-2 N-(4-methyl-1-phenylpentyl)acetamide 
• 1315275-23-0 N-methyl-2-(4-methyl-1-phenylpentylsulfinyl)benzamide 
• 1315275-32-1 C₂₀H₂₅NOS 
• 2527-66-4 2-methyl-1,2-benzisothiazole-3(2H)-one 
• 77334-52-2 1-(4-methoxyphenyl)-4-phenylbutan-1-ol 
• 1315275-28-5 C₂₂H₂₉NO₅ 

Relevant articles and documents

Design, synthesis, and biological testing of thiosalicylamides as a novel class of calcium channel blockers

The current research aimed to investigate the importance of the heterocyclic ring system in the structure of the cardiovascular drug diltiazem for its calcium channel blocking activity. The manuscript describes the design, synthesis, and biological testin

An umpolung sulfoxide reagent for use as a functionalized benzyl carbanion equivalent

N-Methyl ortho-carbamoylaryl benzyl sulfoxides can be used as synthetic equivalents for α-hydroxy, α-chloro, and α-acetammido benzyl carbanions by means of a two-step sequence involving highly diastereoselective α-C-alkylation with alkyl halides followed by displacement of the sulfinyl residue (which can be recovered and recycled) by a hydroxyl, a chlorine or an acetamido, respectively, under non-oxidative Pummerer conditions. The scope and limits of the method, including a stereoselective version of the reaction, as well as the mechanism of the process are discussed in detail.