34239-56-0

Basic information

• Product Name: 2-Propyn-1-one, 1-(3,4-dimethoxyphenyl)-
• CAS NO: 34239-56-0
• Molecular Formula: C11H10O3
• Molecular Weight: 190.199
• Mol File: 34239-56-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Propyn-1-one, 1-(3,4-dimethoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propyn-1-one, 1-(3,4-dimethoxyphenyl)-(34239-56-0)
• EPA Substance Registry System: 2-Propyn-1-one, 1-(3,4-dimethoxyphenyl)-(34239-56-0)

Safety Data

• Hazardous Substances Data: 34239-56-0(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 6953-67-9 1-(3,4-dimethoxyphenyl)prop-2-yn-1-ol 

Downstream Products

• 1187164-00-6 3,4-dimethoxyphenyl(quinolin-3-yl)methanone 
• 1297606-24-6 1-(3,4-dimethoxyphenyl)-2-[(2S,4S)-4-methyl-3-tosyloxazolidin-2-yl]ethanone 
• 1297605-72-1 1-(3,4-dimethoxyphenyl)-2-[(2S,4S)-4-isopropyl-3-tosyloxazolidin-2-yl]ethanone 
• 103650-43-7 2-acetoxy-3-(2-acetoxy-4,6-dimethoxy-phenyl)-1-(3,4-dimethoxy-phenyl)-propan-1-one 
• 102172-58-7 1-(3,4-dimethoxy-phenyl)-3-hydroxy-3-(2-hydroxy-4,6-dimethoxy-phenyl)-propane-1,2-dione 
• 102019-33-0 (3,4-dimethoxy-phenyl)-(2-hydroxy-4,6-dimethoxy-phenyl)-propanetrione 
• 109396-03-4 1-(3,4-dimethoxy-phenyl)-2-hydroxy-3-(2-hydroxy-4,6-dimethoxy-phenyl)-propan-1-one 
• 20052-37-3 3',4',5,7-tetramethoxyflav-2-ene 
• 94143-69-8 2-acetoxy-3',4,4',6-tetramethoxychalcone 

Relevant articles and documents

2,4,6-TRIALKOXYSTRYL ARYL SULFONES, SULFONAMIDES AND CARBOXAMIDES, AND METHODS OF PREPARATION AND USE

Compounds according to Formula (I) are provided and salts thereof, wherein R1, R2, R33, R4, R5, R6, R13, A, X and Y are as defined herein. Methods for preparing compounds of Form

Parallel synthesis of "Click" chalcones as antitubulin agents

It has been shown that some chalcones are able to inhibit tubulin polymerization, giving cytotoxicity and destruction of tumoral vasculature. A library of 180 novel chalcone analogs has been synthesized via click chemistry and screened for their cytotoxic

Straightforward synthesis of highly hydroxylated phloroglucinol-type 3-deoxyanthocyanidins

Phloroglucinol-type 3-deoxyanthocyanidins were synthesized through the interaction between phloroglucinol derivatives and arylethynylketones in acetic acid in the presence of aqueous hexafluorophosphoric acid. This methodology was applied to achieve the synthesis of natural apigeninidin, luteolinidin and tricetanidin with high yields. Georg Thieme Verlag Stuttgart.