72344-13-9

Basic information

• Product Name: 2-Propen-1-one, 3-[4-(methylthio)phenyl]-1-phenyl-
• CAS NO: 72344-13-9
• Molecular Formula: C16H14OS
• Molecular Weight: 254.353
• Mol File: 72344-13-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 3-[4-(methylthio)phenyl]-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 3-[4-(methylthio)phenyl]-1-phenyl-(72344-13-9)
• EPA Substance Registry System: 2-Propen-1-one, 3-[4-(methylthio)phenyl]-1-phenyl-(72344-13-9)

Safety Data

• Hazardous Substances Data: 72344-13-9(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 3446-89-7 4-(Methylthio)benzaldehyde 

Downstream Products

• 72344-14-0 (E)-3-(4-(methylsulfonyl)phenyl)-1-phenylprop-2-en-1-one 
• 72344-04-8 5-(4-methylsulfanyl-phenyl)-1,3-diphenyl-4,5-dihydro-1H-pyrazole 
• 1637672-69-5 5-(4-(methylthio)phenyl)-4,5-dihydro-2H-benzo[g]indazole 
• 1637672-65-1 2-(hydroxymethylene)-4-(4-(methylthio)phenyl)-1,2,3,4-tetrahydronaphthalen-1(2H)-one 
• 1637672-61-7 4-(4-(methylthio)phenyl)-1,2,3,4-tetrahydronaphthalen-1(2H)-one 
• 1637672-57-1 (2-(4-(methylthio)phenyl)cyclopropyl)(phenyl)methanone 
• 1616764-92-1 3-(4-methylthiophenyl)-1-phenyl-5-(2-pyridyl)pentane-1,5-dione 
• 1616765-13-9 2-(2-pyridyl)-4-phenyl-6-(4-methylthiophenyl)phosphinine-P,N-tungsten tetracarbonyl 
• 1616765-01-5 2-(2-pyridyl)-4-(4-methylthiophenyl)-6-phenylphosphinine 
• 1042441-88-2 4-phenyl-2-(4-thiomethylphenyl)-2,3-dihydro-1,5-benzothiazepine 
• 96550-90-2 3-(4-(methylthio)phenyl)-1-phenylpropan-1-one 

Relevant articles and documents

N-para-sulfonium salt substituted pyrazoline derivative, photocurable composition and preparation method

The invention relates to an N-para-sulfonium salt substituted pyrazoline derivative shown as the following formula (I) in the specification, a photocurable composition, and a preparation method of theN-para-sulfonium salt substituted pyrazoline derivative shown as the following formula (I). The N-para-sulfonium salt substituted pyrazoline derivative shown as formula (I) has good absorption at a wavelength of 350nm or above, and compared with a 5-substituted sulfonium salt, the N-para-sulfonium salt substituted pyrazoline derivative has the advantages of simpler and more convenient molecule synthesis steps and reduced cost of raw materials, and is more suitable for industrial production and application.

Proton-Coupled Electron Transfer: Transition-Metal-Free Selective Reduction of Chalcones and Alkynes Using Xanthate/Formic Acid

Highly chemoselective reduction of α,β-unsaturated ketones to saturated ketones and stereoselective reduction of alkynes to (E)-alkenes has been developed under a transition-metal-free condition using a xanthate/formic acid mixture through proton-coupled electron transfer (PCET). Mechanistic experiments and DFT calculations support the possibility of a concerted proton electron-transfer (CPET) pathway. This Birch-type reduction demonstrates that a small nucleophilic organic molecule can be used as a single electron-transfer (SET) reducing agent with a proper proton source.

Synthesis, spectral, biological activity, and crystal structure evaluation of novel pyrazoline derivatives having sulfonamide moiety

In the present study, synthesis and characterization of pyrazoline derivatives integrated with sulfonamide scaffold have been performed. The characterization of the molecules was done by elemental analysis, ultraviolet–visible, infrared, nuclear magnetic