896712-06-4

Basic information

• Product Name: 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde
• Synonyms: 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde
• CAS NO: 896712-06-4
• Molecular Weight: 197.236
• Mol File: 896712-06-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde(896712-06-4)
• EPA Substance Registry System: 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde(896712-06-4)

Safety Data

• Hazardous Substances Data: 896712-06-4(Hazardous Substances Data)

Upstream product

• 58042-93-6 2-phenyl-1-vinyl-1H-pyrrole 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1220056-59-6 (Z)-5-phenyl-1-vinylpyrrole-2-carbaldehyde oxime 
• 1220056-65-4 (E)-5-phenyl-1-vinylpyrrole-2-carbaldehyde oxime 
• 1372648-05-9 2-acetoxy-2-(2-formyl-5-phenyl-1H-pyrrol-1-yl)ethylmercury acetate 
• 52179-74-5 5-phenyl-1H-pyrrole-2-carbaldehyde 
• 1283149-72-3 C₁₃H₁₀Cl₄NOP 
• 1246619-67-9 2-amino-6-{[(5-phenyl-1-vinylpyrrol-2-yl)methylene]amino}hexanoic acid 
• 1204655-20-8 2-(5-phenyl-1-vinyl-1H-pyrrol-2-yl)-1H-benzimidazole 
• 1204655-12-8 N-[(5-phenyl-1-vinyl-1H-pyrrol-2-yl)methylene]benzene-1,2-diamine 
• 1166234-26-9 2-[(5-phenyl-1-vinylpyrrol-2-yl)methylidene]hydrazinecarbothioamide 
• 1166234-31-6 2-[(5-phenyl-1-vinylpyrrol-2-yl)methylidene]hydrazinecarboximidamide 
• 1166234-19-0 2-[(5-phenyl-1-vinylpyrrol-2-yl)methylidene]hydrazinecarboxamide 
• 1108157-58-9 5-phenyl-1-vinyl-1H-pyrrole-2-carbaldehyde oxime 
• 934478-83-8 2-[bis(ethylsulfanyl)methyl]-1-(2-ethylthioethyl)-5-phenylpyrrole 
• 1344663-40-6 (Z)-3-{[(Z)-2-cyano-1-phenylvinyl]oxy}-2-[(1-methyl-1H-imidazol-2-yl)(5-phenyl-1-vinyl-1H-pyrrol-2-yl)methyl]-3-phenylprop-2-enenitrile 

Relevant articles and documents

An efficient route to 1-vinylpyrrole-2-carbaldehydes

1-Vinylpyrroles are formylated by the N-N dimethyl- formamide/oxalyl chloride reagent system (CH2Cl2, r.t., 40 min) to give the corresponding 1-vinylpyrrole-2-carbaldehydes in yields up to 97%. Georg imeme Verlag Stuttgart.

Expedient synthesis of 1-vinylpyrrole-2-carbaldehydes

1-Vinylpyrrole-2-carbaldehydes and 1-vinyl-4,5-dihydrobenzo[g]indole-2-carbaldehyde were synthesized in 56-91% yields from their 1-vinyl derivatives by a modified Vilsmeier-Haack reaction. A low temperature (-78 °C) is required to avoid removal of the N-v