41841-06-9

Basic information

• Product Name: 1-Propanone, 3,3-dimethoxy-1,2-diphenyl-
• CAS NO: 41841-06-9
• Molecular Formula: C17H18O3
• Molecular Weight: 270.328
• Mol File: 41841-06-9.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3,3-dimethoxy-1,2-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3,3-dimethoxy-1,2-diphenyl-(41841-06-9)
• EPA Substance Registry System: 1-Propanone, 3,3-dimethoxy-1,2-diphenyl-(41841-06-9)

Safety Data

• Hazardous Substances Data: 41841-06-9(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 94-41-7 benzalacetophenone 
• 67-56-1 methanol 
• 89959-83-1 1,3-diphenyl-2,3-bis(tosyloxy)-1-oxopropane 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 149-73-5 trimethyl orthoformate 
• 33266-45-4 Formyldesoxybenzoin 

Downstream Products

• 36372-77-7 1,4,5-triphenyl-1H-pyrazole 
• 451-40-1 phenyl benzyl ketone 

Relevant articles and documents

Synthesis, characterisation, and reactivity of novel pseudocyclic hypervalent iodine reagents with heteroaryl carbonyl substituents

Two new hypervalent iodine reagents containing furan and thiophene moieties in addition to a carbonyl group in the vicinity of the iodine atom were synthesised and characterised. The X-ray analysis of both compounds revealed a strong intramolecular contact between the carbonyl oxygen and the hypervalent iodine atom with tosylate as a counter ion. The two reagents showed a broad range of synthetic applications and proved to be versatile oxidizing agents.

Preparation, structure, and versatile reactivity of pseudocyclic benziodoxole triflate, new hypervalent iodine reagent

A new pseudocyclic triflate derivative of benziodoxole (IBA-OTf) was prepared and characterized by X-ray analysis. This highly electrophilic reagent readily reacts with various organic substrates to give the corresponding products in good yields. Furthermore, IBA-OTf can be used as a catalyst with m-chloroperoxybenzoic acid as the terminal oxidant. This journal is

The chemistry of α,β-ditosyloxyketones: Novel routes for the synthesis of desoxybenzoins and α-aryl-β-ketoaldehyde dimethylacetals from α,β-chalcone ditosylates

The reaction of α,β-chalcone ditosylates 3 with potassium hydroxide in suitable conditions leads to 1,2-aryl shift and carbon-carbon bond cleavage, thereby providing a novel route for the synthesis of 1,2-diarylethan-1-ones 4 and 1,2-diaryl-3,3-dimethoxy propan-1-ones 5. Georg Thieme Verlag Stuttgart.