1256262-90-4

Basic information

• Product Name: tert-butyl (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylate
• Synonyms: tert-butyl (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylate
• CAS NO: 1256262-90-4
• Molecular Weight: 272.344
• Mol File: 1256262-90-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: tert-butyl (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylate(1256262-90-4)
• EPA Substance Registry System: tert-butyl (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylate(1256262-90-4)

Safety Data

• Hazardous Substances Data: 1256262-90-4(Hazardous Substances Data)

Upstream product

• 1663-39-4 tert-Butyl acrylate 
• 6630-33-7 ortho-bromobenzaldehyde 
• 1439-36-7 1-triphenylphosphoranylidene-2-propanone 
• 643-79-8 o-phthalic dicarboxaldehyde 
• 86302-43-4 (tert-Butoxycarbonylmethylene)triphenylphosphorane 
• 103890-69-3 (E)-3-(2-formylphenyl)-2-propenoic acid 1,1-dimethylethylester 

Downstream Products

• 1256262-96-0 (E)-3-(2-((E)-3-oxobut-1-en-1-yl)phenyl)acrylic acid 

Relevant articles and documents

Synthesis of Oxatricyclooctanes via Photoinduced Intramolecular Oxa-[4+2] Cycloaddition of Substituted o-Divinylbenzenes

The photolysis of substituted o-divinylbenzenes promotes a one-step and metal-free conversion to oxatricycles at room temperature. Irradiation o-divinylbenzenes results in an pericyclic reaction to form cyclic o-quinodiemthane intermediates, which subsequently undergo intramolecular oxa-[4+2] cycloaddition to form oxacyclic derivatives.

Synthesis of nonsymmetric divinylarenes by a heck/wittig reaction combination

A protocol for a one-pot Heck reaction/Wittig olefination to divinylarenes has been developed. Copyright Taylor & Francis Group, LLC.