42174-01-6

Basic information

• Product Name: 2-Propenoic acid, 3-(2,4-dichlorophenyl)-, methyl ester
• CAS NO: 42174-01-6
• Molecular Formula: C10H8Cl2O2
• Molecular Weight: 231.078
• Mol File: 42174-01-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-(2,4-dichlorophenyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-(2,4-dichlorophenyl)-, methyl ester(42174-01-6)
• EPA Substance Registry System: 2-Propenoic acid, 3-(2,4-dichlorophenyl)-, methyl ester(42174-01-6)

Safety Data

• Hazardous Substances Data: 42174-01-6(Hazardous Substances Data)

Upstream product

• 5927-18-4 trimethyl phosphonoacetate 
• 874-42-0 2,4-dichlorobenzaldeyhde 
• 67-56-1 methanol 
• 20595-45-3 2,4-dichlorocinnamic acid 
• 292638-85-8 acrylic acid methyl ester 
• 29898-32-6 2,4-dichloro-1-iodo-benzene 
• 1067-74-9 Methyl diethylphosphonoacetate 
• 96-32-2 bromoacetic acid methyl ester 
• 186581-53-3 diazomethane 

Downstream Products

• 1207950-18-2 C₁₅H₁₆Cl₂O₆ 
• 1338378-19-0 4-chloro-5-(2,4-dichlorophenyl)-3-ethoxy-1-phenyl-1H-pyrazole 
• 1338378-33-8 5-(2,4-dichlorophenyl)-1-phenyl-1H-pyrazol-3-ol 
• 1338378-34-9 5-(2,4-dichlorophenyl)-3-ethoxy-1-phenyl-1H-pyrazole 
• 1338378-16-7 4-chloro-5-(2,4-dichlorophenyl)-1-phenyl-1H-pyrazol-3-ol 
• 1588522-41-1 C₁₄H₁₃Cl₂NO₄ 
• 6974-65-8 (2,4-dichloro-phenyl)-propynoic acid 
• 1312928-25-8 7-(2,4-dichlorophenyl)-6,7-dihydro-[1,2,4]triazolo[1,5-a]pyrimidin-5(4H)-one 
• 1027496-33-8 3-Cyano-4-[3-(2,4-dichloro-phenyl)-propylsulfanyl]-3-hydroxy-butyric acid methyl ester 
• 1026639-62-2 4-[3-(2,4-Dichloro-phenyl)-propylsulfanyl]-3-oxo-butyric acid methyl ester 
• 1026334-46-2 Thioacetic acid S-[3-(2,4-dichloro-phenyl)-propyl] ester 
• 93962-66-4 1-(3-Bromo-propyl)-2,4-dichloro-benzene 
• 146882-07-7 3-(2,4-dichlorophenyl)propan-1-ol 
• 1504-59-2 3-(2.4-Dichlor-phenyl)-prop-2-en-1-ol 

Relevant articles and documents

Dehydrozingerone derivative and preparation method and application thereof

The invention provides a dehydrozingerone derivative as shown in the description. R-R are each independently selected from hydrogen or halogen or a nitro group or an alkyl group or a substitutedalkoxy group or an alkoxy group or a hydroxyl group; the substituent in the substituted alkoxy group is selected from one or multiple of halogen, a nitro group and a hydroxyl group; R and R areeach independently selected from hydrogen or halogen or nitrogen-containing heterocycle; R is selected from an alkyl group or an alkoxy group or a substituted alkoxy group; the substituent in thesubstituted alkyl group is selected from one or multiple of halogen, a nitro group and a hydroxyl group; X is selected from a hetero atom or a hydroxylamine group. The dehydrozingerone derivative hasbroad-spectrum activity against plant pathogenic fungi and bacteria, and has certain nematicidal activity, and is a lead compound with the broad biological activity.

Hydrogen Peroxide Promoted Mizoroki-Heck Reactions of Phenyldiazenes with Acrylates, Acrylamides, and Styrenes

Mizoroki-Heck reactions, which are well-known for aryldiazonium salts and which have recently been described for arylhydrazines, have now been extended to phenyldiazenes. In situ generation of phenyldiazenes from azocarboxylates allowed clean and selective reactions with styrenes, acrylates, and acrylamides using palladium(II) acetate in the presence of silver(I) acetate or hydrogen peroxide as oxidant. Hydrogen peroxide was thereby shown to be a cheap and broadly applicable alternative for the established palladium-silver(I) system.

Design, synthesis and biological evaluation of novel aminomethyl- piperidones based DPP-IV inhibitors

A series of novel aminomethyl-piperidones were designed and evaluated as potential DPP-IV inhibitors. Optimized analogue 12v ((4S,5S)-5-(aminomethyl)-1- (2-(benzo[d][1,3]dioxol-5-yl)ethyl)-4-(2,5-difluorophenyl)piperidin-2-one) showed excellent in vitro p