56438-64-3

Basic information

• Product Name: 2-Propanone, 1,3-bis(3-methoxyphenyl)-
• CAS NO: 56438-64-3
• Molecular Formula: C17H18O3
• Molecular Weight: 270.328
• Mol File: 56438-64-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Propanone, 1,3-bis(3-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propanone, 1,3-bis(3-methoxyphenyl)-(56438-64-3)
• EPA Substance Registry System: 2-Propanone, 1,3-bis(3-methoxyphenyl)-(56438-64-3)

Safety Data

• Hazardous Substances Data: 56438-64-3(Hazardous Substances Data)

Upstream product

• 4755-77-5 Ethyl oxalyl chloride 
• 824-98-6 m-methoxybenzyl chloride 
• 541-41-3 chloroformic acid ethyl ester 
• 38622-91-2 [(p-methylphenyl)sulfonylmethyl]isonitrile 
• 6834-42-0 3-methoxyphenylacetic acid chloride 
• 1798-09-0 m-methoxyphenylacetic acid 
• 63075-61-6 (3-methoxy-phenyl)-acetic acid-anhydride 
• 19924-43-7 3-methoxyphenylacetonitrile 

Downstream Products

• 1408319-77-6 (Z)-2-((4,5-bis(4-butylphenyl)-3-(3-methoxyphenyl)-2H-pyrrol-2-ylidene)(3-methoxyphenyl)methyl)-4,5-bis(4-butylphenyl)-3-(3-methoxyphenyl)-1H-pyrrole 
• 1386995-37-4 (Z)-3-(3-methoxyphenyl)-2-((3-methoxyphenyl)(3-(3-methoxyphenyl)-4,5-diphenyl-2H-pyrrol-2-ylidene)methyl)-4,5-diphenyl-1H-pyrrole 
• 1386995-35-2 2,5-bis-(3-methoxy-phenyl)-3,4-diphenyl-cyclopenta-2,4-dienone 
• 1408319-71-0 3,4-bis(4-butylphenyl)-2,5-bis(3-methoxyphenyl)cyclopenta-2,4-dienone 
• 51053-85-1 3-methoxybenzyl radical 

Relevant articles and documents

From Alkyl Halides to Ketones: Nickel-Catalyzed Reductive Carbonylation Utilizing Ethyl Chloroformate as the Carbonyl Source

Ketones are an important class of molecules in synthetic and medicinal chemistry. Rapid and modular synthesis of ketones remains in high demand. Described here is a nickel-catalyzed three-component reductive carbonylation method for the synthesis of dialkyl ketones. A wide range of both symmetric and asymmetric dialkyl ketones can be accessed from alkyl halides and a safe CO source, ethyl chloroformate. The approach offers complementary substrate scope to existing carbonylation methods while avoiding the use of either toxic CO or metal carbonyl reagents.

Preparation method of 1,3-disubstituted alkyl phenylacetone

The invention relates to a preparation method of 1,3-disubstituted alkyl phenylacetone and belongs to the field of medical technology and photoelectric materials. The preparation method includes: allowing alkyl phenylacetic acid to have reaction with DMAP

ACTIVATED METALLIC NICKEL IN PREPARATION OF SYMMETRICAL 1,3-DIARYLPROPAN-2-ONES FROM BENZYLIC HALIDES AND OXALYL CHLORIDES

Oxidative addition of benzylic halides to nickel in the metallic state followed by insertion of carbon monoxide generated from alkyl oxalyl chlorides proceeded smoothly to give symmetrical 1,3-diarylpropan-2-ones in moderate yields.