36943-39-2

Basic information

• Product Name: AKOS DM0360
• Synonyms: AKOS DM0360;2-(Phenylthio)Benzaldehyde;2-(Phenylsulfanyl)benzaldehyde;o-Phenylthiobenzaldehyde
• CAS NO: 36943-39-2
• Molecular Formula: C₁₃H₁₀OS
• Molecular Weight: 214.28
• Mol File: 36943-39-2.mol
• Article Data: 43

Chemical Properties

• Melting Point: 50℃
• Boiling Point: 330℃
• Flash Point: 169℃
• Appearance: /
• Density: 1.20
• CAS DataBase Reference: AKOS DM0360(CAS DataBase Reference)
• NIST Chemistry Reference: AKOS DM0360(36943-39-2)
• EPA Substance Registry System: AKOS DM0360(36943-39-2)

Safety Data

• Hazardous Substances Data: 36943-39-2(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 446-52-6 2-Fluorobenzaldehyde 
• 6630-33-7 ortho-bromobenzaldehyde 
• 882-33-7 diphenyldisulfane 
• 459-57-4 4-fluorobenzaldehyde 
• 40138-16-7 2-formylbenzene boronic acid 
• 873-55-2 sodium benzenesulfonate 
• 100-52-7 benzaldehyde 
• 90-02-8 salicylaldehyde 
• 98-80-6 phenylboronic acid 
• 552-89-6 2-nitro-benzaldehyde 
• 639-58-7 triphenyltin chloride 
• 555-16-8 4-nitrobenzaldehdye 
• 4551-15-9 phenylthiotrimethylsilane 

Downstream Products

• 352427-00-0 2-(Phenylsulfanyl)benzaldehyde oxime 
• 66571-98-0 3-propyl-9-(2,3,5,6-tetramethyl-phenyl)-thioxanthene 
• 90133-44-1 9-mesitylthioxanthene 10-oxide 
• 90133-40-7 3,6-dimethyl-9-mesitylthioxanthene 
• 90133-43-0 9-methyl-9-(2,3,4-trimethylphenyl)thioxanthene 
• 90133-45-2 9-durylthioxanthene 10-oxide 
• 90133-54-3 9-mesityl-9-(p-methoxyphenyl)thioxanthene 
• 72751-73-6 3-Propyl-9-(2,4,6-trimethyl-phenyl)-9H-thioxanthene 10,10-dioxide 
• 72731-25-0 3-Propyl-9-(2,3,5,6-tetramethyl-phenyl)-9H-thioxanthene 10,10-dioxide 
• 90133-53-2 9-mesityl-thioxanthylium perchlorate 
• 90133-49-6 9-duryl-thioxanthylium perchlorate 
• 90133-47-4 9-mesityl-10-(p-methoxyphenyl)thioxanthenium perchlorate 
• 90133-42-9 trans-10-methyl-9-(2,3,4-trimethylphenyl)thioxanthenium perchlorate 
• 91127-71-8 cis-10-methyl-9-(2,3,4-trimethylphenyl)thioxanthenium perchlorate 

Relevant articles and documents

Synthesis and biological activity of sulfur-containing aryl-aldehyde Schiff bases.

A series of chemically modified aryl-aldehyde Schiff bases has been synthesized and tested for their antioxidant activity and radiation protection. We observed that disulfide-containing aryl-aldehyde Schiff base 6c exhibited potent free radical scavenging

Chan-Lam-Type C-S Coupling Reaction by Sodium Aryl Sulfinates and Organoboron Compounds

A Chan-Lam-Type C-S coupling reaction using sodium aryl sulfinates has been developed to provide diaryl thioethers in up to 92% yields in the presence of a copper catalyst and potassium sulfite. Both electron-rich and electron-poor sodium aryl sulfinates and diverse organoboron compounds were tolerated for the synthesis of aryl and heteroaryl thioethers and dithioethers. The mechanistic study suggested that potassium sulfite was involved in the deoxygenation of sulfinate through a radical process.

Cerium-photocatalyzed aerobic oxidation of benzylic alcohols to aldehydes and ketones

We have developed a cerium-photocatalyzed aerobic oxidation of primary and secondary benzylic alcohols to aldehydes and ketones using inexpensive CeCl3 7H2O as photocatalyst and air oxygen as the terminal oxidant.