37913-72-7

Basic information

• Product Name: (1E,3E)-1-(2-Thienyl)-4-phenyl-1,3-butadiene
• Synonyms: (1E,3E)-1-(2-Thienyl)-4-phenyl-1,3-butadiene;(1E,3E)-1-Phenyl-4-(2-thienyl)-1,3-butadiene;2-(4-Phenyl-buta-1,3-dienyl)-thiophene
• CAS NO: 37913-72-7
• Molecular Formula: C₁₄H₁₂S
• Molecular Weight: 212.31
• Mol File: 37913-72-7.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1E,3E)-1-(2-Thienyl)-4-phenyl-1,3-butadiene(CAS DataBase Reference)
• NIST Chemistry Reference: (1E,3E)-1-(2-Thienyl)-4-phenyl-1,3-butadiene(37913-72-7)
• EPA Substance Registry System: (1E,3E)-1-(2-Thienyl)-4-phenyl-1,3-butadiene(37913-72-7)

Safety Data

• Hazardous Substances Data: 37913-72-7(Hazardous Substances Data)

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 2243-53-0 styrylacetic acid 
• 39511-11-0 (E)-1-phenyl-3-(thiophen-2-yl)-2-propen-1-one 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 14756-03-7 3-(2-thienyl)acrolein 
• 103-82-2 phenylacetic acid 

Downstream Products

• 103437-34-9 C₃₄H₂₀S₂ 
• 103348-58-9 C₃₄H₂₀S₂ 
• 103348-57-8 Dichlor-2-phenyl-5(2-thienyl)-bicyclo<4.1.0>hepta-1,3,5-trien 
• 103348-56-7 2-(1,6,7,7-Tetrachloro-5-phenyl-bicyclo[4.1.0]hept-3-en-2-yl)-thiophene 

Relevant articles and documents

Indium triflate catalyzed rearrangement of aryl-substituted cyclopropyl carbinols to 1,4-disubstituted 1,3-butadienes

Aryl-substituted cyclopropyl carbinol derivatives undergo a facile stereoselective rearrangement catalyzed by In(OTf)3 in dichloromethane under sonication to produce the substituted conjugated all-trans-butadienes. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

THE ONE-POT PALLADIUM CATALYZED WITTIG REACTION WITH ALLYLIC ALCOHOLS. SCOPE AND LIMITATIONS

Some allylic alcohols react with aldehydes and triphenylphosphine in a one-pot formal Wittig reaction under Pd0 catalysis.The method has been extended to cinnamyl alcohol, 1, 2-methyl-2-propen-1-ol, 7, and 3-buten-2-ol, 11, and to heterocyclic aldehydes.