93351-44-1

Basic information

• Product Name: 3-(3-METHOXYPHENOXY)-2-BUTANONE
• Synonyms: 3-(3-METHOXYPHENOXY)-2-BUTANONE
• CAS NO: 93351-44-1
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 93351-44-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(3-METHOXYPHENOXY)-2-BUTANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-METHOXYPHENOXY)-2-BUTANONE(93351-44-1)
• EPA Substance Registry System: 3-(3-METHOXYPHENOXY)-2-BUTANONE(93351-44-1)

Safety Data

• Hazardous Substances Data: 93351-44-1(Hazardous Substances Data)

Upstream product

• 150-19-6 O-methylresorcine 
• 4091-39-8 3-chloro-2-butanone 
• 1122-95-8 sodium 4-methoxyphenolate 
• 814-75-5 3-bromo-butanone 

Downstream Products

• 231300-46-2 (E)-1-(6-Hydroxy-2,3-dimethyl-benzofuran-5-yl)-3-(3,4,5-trimethoxy-phenyl)-propenone 
• 231300-47-3 (E)-1-(6-Hydroxy-2,3-dimethyl-benzofuran-5-yl)-3-(4-methoxy-phenyl)-propenone 
• 231300-49-5 (E)-1-(6-Hydroxy-2,3-dimethyl-benzofuran-5-yl)-3-(3-methoxy-phenyl)-propenone 
• 231300-44-0 (E)-1-(6-Hydroxy-2,3-dimethyl-benzofuran-5-yl)-3-phenyl-propenone 

Relevant articles and documents

Enantioselective Construction of Chiral 2,3-cis-Dimethyldihydrobenzofuran with an All-Carbon Quaternary Center: An Efficient Approach to (+)/(-)-PI-220 and (+)-3-epi-Furaquinocin C

A new strategy for the enantioselective construction of chiral 2,3-cis-dimethyldihydrobenzofurans has been developed by a ruthenium-catalyzed asymmetric hydrogenation of racemic α-aryloxybutanone via dynamic kinetic resolution (DKR), combined with a palladium-catalyzed intramolecular reductive Heck cyclization. Starting from optically active 2,3-cis-dimethyldihydrobenzofuran, the natural products (+)/(-)-PI-220 and (+)-3-epi-furaquinocin C were synthesized in high yields.

Dihydrothienopsoralens: New furocoumarins as potential photoreacting agents

A series of new dihydrothienopsoralen derivatives were synthesized from 6-hydroxybenzo[b]furan in four steps in good yield. These compounds were prepared as potential photosensitizing and chemotherapeutic agents for psoriasis. The spectroscopy study in al