1219452-59-1

Basic information

• Product Name: 4-Pentenoic acid, 5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylene-, methyl ester, (4Z)-
• CAS NO: 1219452-59-1
• Molecular Formula: C13H12Cl2O3
• Molecular Weight: 287.142
• Mol File: 1219452-59-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-Pentenoic acid, 5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylene-, methyl ester, (4Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pentenoic acid, 5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylene-, methyl ester, (4Z)-(1219452-59-1)
• EPA Substance Registry System: 4-Pentenoic acid, 5-chloro-5-(4-chlorophenyl)-3-hydroxy-2-methylene-, methyl ester, (4Z)-(1219452-59-1)

Safety Data

• Hazardous Substances Data: 1219452-59-1(Hazardous Substances Data)

Upstream product

• 99-91-2 para-chloroacetophenone 
• 14063-77-5 (Z)-3-chloro-3-(4-chlorophenyl)acrylaldehyde 
• 292638-85-8 acrylic acid methyl ester 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1204966-43-7 methyl (2Z,4Z)-2-(bromomethyl)-5-chloro-5-(4-chlorophenyl)penta-2,4-dienoate 
• 1242316-85-3 methyl (2E,4Z)-2-(bromomethyl)-5-chloro-5-(4-chlorophenyl)penta-2,4-dienoate 
• 1219452-49-9 (2Z,4Z)-methyl 5-chloro-2-(chloromethyl)-5-(4-chlorophenyl)penta-2,4-dienoate 
• 1361123-78-5 (2E,4Z)-methyl-5-chloro-5-(4-chlorophenyl)-2-(hydroxymethyl)penta-2,4-dienoate 

Relevant articles and documents

Unexpected tandem reaction of new type moritabaylis- Hillman adducts promoted by [HMIM]HSO4/NANO3 system

A tandem reaction of new type Baylis-Hillman adducts 1 was prompted by ionic liquid [Hmim]HSO4/NaNO3 system and the unexpected products 6-aryl-2H-pyran-3-carboxylates 2 and imidazolium salts 3 were efficiently formed via the rearrang

One-pot synthesis of new type aza- Baylis-Hillman adducts from chlorovinyl aldehydes under solvent-free condition

A series of new type aza- Baylis-Hillman adducts were prepared in moderate yields by one-pot treatment of chlorovinyl aldehydes, benzenesulfonamides and activated olefi ns under solvent-free condition. The chlorovinyl aldehydes were obtained via chlorofor