364633-47-6

Basic information

• Product Name: methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate
• Synonyms: methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate
• CAS NO: 364633-47-6
• Molecular Weight: 261.105
• Mol File: 364633-47-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate(364633-47-6)
• EPA Substance Registry System: methyl 3-(2,4-dichlorophenyl)-3-hydroxy-2-methylenepropanoate(364633-47-6)

Safety Data

• Hazardous Substances Data: 364633-47-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 5445-17-0 Methyl 2-bromopropionate 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 364633-51-2 (E)-3-(2,4-Dichloro-phenyl)-2-methyl-acrylic acid methyl ester 
• 1589493-46-8 (E)-methyl 3-(2,4-dichlorophenyl)-2-((N-(2-formylphenyl)-4-methylphenylsulfonamido)methyl)acrylate 
• 1010833-16-5 (5Z)-2-amino-[5-(2,4-dichlorobenzylidene)]-5,6-dihydro-1,3-thiazin-4-one 
• 1247015-89-9 (E)-methyl 2-(aminomethyl)-3-(2,4-dichlorophenyl)acrylate 
• 1367876-36-5 C₁₀H₈Cl₂O₂ 
• 103754-42-3 -3-(2,4-dichlorophenyl)-2-methylprop-2-enoic acid 
• 1367876-27-4 [(Z)-3-(2,4-dichlorophenyl)-2-methoxycarbonyl-2-propenyl]triphenylphosphonium bromide 

Relevant articles and documents

Novel Sc(OTf)3/3-HQD catalyst for Morita-Baylis-Hillman reaction

A novel and efficient catalytic system of the Morita-Baylis-Hillman (MBH) reaction between aromatic aldehyde and activated alkenes has been developed. The novel system of a combination of Sc(OTf)3 and 3-hydroxyquinuclidine (3-HQD) showed a high catalytic

Synthesis of 1,3-thiazine-2,4-diones with potential anticancer activity

2-Amino-1,3-thiazin-4-ones were subjected to acetylation followed by mild acid hydrolysis to give compounds containing the 1,3-thiazine-2,4-dione core. The potential of these S,N-containing heterocycles as antitumor agents against human cancer cell lines,

Iodine-mediated intramolecular electrophilic aromatic cyclization in allylamines: A general route to synthesis of quinolines, pyrazolo[4,3-b] pyridines, and thieno[3,2-b]pyridines

An unprecedented synthesis of aromatic ring annulated pyridines from suitably substituted primary allylamines via intramolecular electrophilic aromatic cyclization mediated by molecular iodine under mild conditions is described.