422268-02-8

Basic information

• Product Name: (Z)-but-2-ene-1,4-diyl bis-(4-methoxybenzoate)
• Synonyms: (Z)-but-2-ene-1,4-diyl bis-(4-methoxybenzoate)
• CAS NO: 422268-02-8
• Molecular Weight: 356.375
• Mol File: 422268-02-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (Z)-but-2-ene-1,4-diyl bis-(4-methoxybenzoate)(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-but-2-ene-1,4-diyl bis-(4-methoxybenzoate)(422268-02-8)
• EPA Substance Registry System: (Z)-but-2-ene-1,4-diyl bis-(4-methoxybenzoate)(422268-02-8)

Safety Data

• Hazardous Substances Data: 422268-02-8(Hazardous Substances Data)

Upstream product

• 6117-80-2 1,4-butenediol 
• 100-07-2 4-methoxy-benzoyl chloride 

Downstream Products

• 1155875-32-3 2-(4-tolyl)but-3-en-1-ol 
• 42238-17-5 (Z)-4-p-Tolyl-but-2-en-1-ol 
• 1155875-26-5 C₁₉H₂₀O₃ 
• 1431559-27-1 (5S,6R)-7-((tert-butyldiphenylsilyl)oxy)-5,6-dihydroxyhept-2-en-1-yl 4-methoxybenzoate 
• 1431559-42-0 (5R,6R)-7-((tert-butyldiphenylsilyl)oxy)-5,6-dihydroxyhept-2-en-1-yl 4-methoxybenzoate 
• 1260868-76-5 (E)-5-hydroxy-5-phenylpent-2-enyl 4-methoxybenzoate 
• 1161828-01-8 2-ethylbut-3-enyl 4-methoxybenzoate 

Relevant articles and documents

Concise synthesis of tetrahydropyrans by a tandem oxa-michael/tsuji-trost reaction

A novel domino sequence facilitates the rapid assembly of polysubstituted tetrahydropyrans. The one-pot relay process generates up to three new stereogenic centers, including a tetrasubstituted carbon center, in a highly concise and convergent fashion from simple starting materials. Copyright

Synthesis of homoallylic alcohols via lewis acid assisted enantioselective desymmetrization

A highly enantioselective allylic substitution of (Z)-but-2-ene-1,4-diol derivatives was developed using a rhodium(I) catalyst and arylboronic acids as nucleophiles. The reaction yields versatile homoallylic alcohols from readily available linear biscarbonates. Georg Thieme Verlag Stuttgart.