233669-44-8

Basic information

• Product Name: (E)-1-(2-Benzoyl-6-hydroxy-3-methyl-benzofuran-5-yl)-3-(2-chloro-phenyl)-propenone
• Synonyms: (E)-1-(2-Benzoyl-6-hydroxy-3-methyl-benzofuran-5-yl)-3-(2-chloro-phenyl)-propenone
• CAS NO: 233669-44-8
• Molecular Weight: 416.861
• Mol File: 233669-44-8.mol

Chemical Properties

• CAS DataBase Reference: (E)-1-(2-Benzoyl-6-hydroxy-3-methyl-benzofuran-5-yl)-3-(2-chloro-phenyl)-propenone(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(2-Benzoyl-6-hydroxy-3-methyl-benzofuran-5-yl)-3-(2-chloro-phenyl)-propenone(233669-44-8)
• EPA Substance Registry System: (E)-1-(2-Benzoyl-6-hydroxy-3-methyl-benzofuran-5-yl)-3-(2-chloro-phenyl)-propenone(233669-44-8)

Safety Data

• Hazardous Substances Data: 233669-44-8(Hazardous Substances Data)

Upstream product

• 70-11-1 α-bromoacetophenone 
• 2161-85-5 1-(5-acetyl-2,4-dihydroxyphenyl)-1-ethanone 
• 89-98-5 2-chloro-benzaldehyde 
• 106206-62-6 5-acetyl-2-benzoyl-6-hydroxy-3-methylbenzo[b]furan 

Downstream Products

• 1400900-20-0 C₂₅H₁₆Cl₂O₃ 
• 198343-10-1 {5-[2-(2-Chloro-phenyl)-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl]-6-hydroxy-3-methyl-benzofuran-2-yl}-phenyl-methanone 

Relevant articles and documents

Microwave assisted synthesis of [5-chloro-3-methyl-7-aryl-7H-furo [3,2-g] chromen-2-yl] (phenyl) methanones and their antibacterial activity

A series of [5-chloro-3-methyl-7-aryl-7H-furo [3,2-g] chromen-2-yl] (phenyl) methanones (llla-g) have been prepared by the reaction of (E)-1 -(2-benzoyl-6-hydroxy-3-methyl benzo [b] furan-5-yl)-3-aryl-2-propen-1-ones (lla-g) with Vilsmeier-Haack reagent u

A facile synthesis of 2,6-dibenzoyl-5-methyl-3-(substituted styryl)-benzo[1,2-b;5,4-b']difurans under phase transfer catalytic conditions and their antifeedant activity

2,6-Dibenzoyl-5-methyl-3-(substituted styryl) benzo[1,2-b;5,4-b']difurans 4a-i have been prepared by condensing 2-benzoyl-5-substituted cinnamoyl-6-hydroxy-3-methylbenzofurans 3a-i with 2-bromoacetophenone under phase transfer catalytic conditions. All th

An efficient procedure for the preparation of 3'-acetyl-2',3'- dihydrobenzothiazoles by ring contraction of 2',3'-dihydro-1,5- benzothiazepines under acetylating conditions

Reaction of 2-benzoyl-6-hydroxy-3-methyl-5-(2'-substituted-2',3'- dihydro-1,5-benzothiazepin-4'-yl) benzofurans (4a-f) with a mixture of acetic anhydride and pyridine afforded 6-acetoxy-2-benzoyl-3-methyl-5-(3'-acetyl-2'- substitutedstyryl-2',3'-dihydrobe

A facile synthesis of 2-benzoyl-6-hydroxy-3-methyl-5-(2-substituted-2,3- dihydro-1H-1,5-benzodiazepin-4-yl) benzo[b]furans

The synthesis and characterisation of some new 1,5-benzodiazepines prepared from 4,6-diacetykesorcinol is reported.

A facile synthesis of 7-(substituted aryl)-2-benzoyl-3-methyl-5H-furo[3,2-g] [1]benzopyran-5-ones and their antifeedant activity

The synthesis, characterisation and antifeedant activity of some new furochromones prepared from 4,6-diacetylresorcinol have been reported.

A facile synthesis of 2-benzoyl-6-hydroxy-3-methyl-5-(4',5'-dihydro-5'- aryl pyrazol-3'-yl) benzofurans

The synthesis, and characterisation of some new pyrazolines prepared from 4,6-diacetylresorcinol is reported.

A facile synthesis of 2-benzoyl-6-hydroxy-3-methyl-5-(2'-substituted- 2',3'-dihydro- 1,5-benzothiazepin- 4'-yl)benzofurans and their antifeedant activity

The synthesis, characterisation and antifeedant activity of some new 1,5-benzothiazepines prepared from 4,6-diacetylresorcinol has been reported.

A facile synthesis of 2-benzoyl-3-methyl-6-phenyl-5-(substituted styryl)-7H-furo [3,2-g] [1] benzopyran-7-ones and their antifeedant activity

The synthesis, characterisation and antifeedant activity of some new furocoumarins prepared from 4,6-diacetyl resorcinol has been reported.