24393-66-6

Basic information

• Product Name: ethyl (E)-3-(1,3-benzodioxol-5-yl)acrylate
• Synonyms: 3-(1,3-Benzodioxol-5-yl)-2-propenoic acid ethyl ester;3-(1,3-benzodioxol-5-yl)acrylic acid ethyl ester;3-(1,3-benzodioxol-5-yl)prop-2-enoic acid ethyl ester;Ethyl (2E)-3-;ethyl (2E)-3-(1,3-benzodioxol-5-yl)acrylate;ethyl (E)-3-(1,3-benzodioxol-5-yl)prop-2-enoate;ethyl 3-(1,3-benzodioxol-5-yl)prop-2-enoate;ethyl (E)-3-(1,3-benzodioxol-5-yl)acrylate
• CAS NO: 24393-66-6
• Molecular Formula: C₁₂H₁₂O₄
• Molecular Weight: 220.22128
• EINECS: 246-220-2
• Mol File: 24393-66-6.mol
• Article Data: 53

Chemical Properties

• Melting Point: 51-53 °C
• Boiling Point: 337.2°Cat760mmHg
• Flash Point: 149.2°C
• Appearance: /
• Density: 1.236g/cm³
• Vapor Pressure: 0.000106mmHg at 25°C
• Refractive Index: 1.58
• CAS DataBase Reference: ethyl (E)-3-(1,3-benzodioxol-5-yl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (E)-3-(1,3-benzodioxol-5-yl)acrylate(24393-66-6)
• EPA Substance Registry System: ethyl (E)-3-(1,3-benzodioxol-5-yl)acrylate(24393-66-6)

Safety Data

• Hazardous Substances Data: 24393-66-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H12O4/c1-2-14-12(13)6-4-9-3-5-10-11(7-9)16-8-15-10/h3-7H,2,8H2,1H3/b6-4+

Upstream product

• 274-09-9 Methylenedioxybenzene 
• 140-88-5 ethyl acrylate 
• 495-76-1 piperonol 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 120-57-0 piperonal 
• 5764-82-9 bromo(2-ethoxy-2-oxoethyl)zinc 
• 105-36-2 ethyl bromoacetate 
• 311-46-6 ethyl 2-(dimethoxyphosphoryl)acetate 
• 133505-33-6 carbethoxymethyldibutyltelluronium bromide 
• 64-17-5 ethanol 
• 141-82-2 malonic acid 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 2620-50-0 1,3-benzodioxol-5-ylmethyl amine 
• 31930-36-6 ethyl (Z)-3-iodopropenoate 

Downstream Products

• 7116-48-5 3-benzo[1,3]dioxol-5-yl-propionic acid ethyl ester 
• 2373-80-0 3,4-methylenedioxy-trans-cinnamic acid 
• 112778-62-8 (2S,3S)-2-Benzo[1,3]dioxol-5-yl-5-(3,4-dimethoxy-phenyl)-2,3-dihydro-furan-3,4-dicarboxylic acid diethyl ester 
• 133701-82-3 (5-ethoxycarbonyl-4-hydroxy-c-2,t-6-bis(3,4-methylenedioxyphenyl)-t-3-phenylcyclohex-4-ene-r-1,3-carbolactone) 
• 58095-76-4 (E)-3-(benzo[d][1,3]dioxol-5-yl)prop-2-en-1-ol 
• 149520-09-2 (S)-(-)-ethyl 3-amino-3-[5-(benzo-1,3-dioxole)]propanoate 
• 580-73-4 (+/-)-hinokinin 
• 40456-51-7 (3S,4S)-4-(benzo[d][1,3]dioxol-5-ylmethyl)-3-(3,4-dimethoxybenzyl)dihydrofuran-2(3H)-one 

Relevant articles and documents

Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

The Fujiwara-Moritani reaction has had a profound contribution in the emergence of contemporary C-H activation protocols. Despite the applicability of the traditional approach in different fields, the associated reactivity and regioselectivity issues had

Metal-free domino Cloke-Wilson rearrangement-hydration-dimerization of cyclopropane carbaldehydes: A facile access to oxybis(2-aryltetrahydrofuran) derivatives

In this work, we have demonstrated a metal-free transformation of cyclopropane carbaldehydes to oxybis(2-aryltetrahydrofuran) derivatives via a domino Cloke-Wilson rearrangement-hydration-dimerization sequence. Commercially inexpensive p-toluene sulfonic acid (PTSA) was used as a Br?nsted acid catalyst, and reactions were conducted in an open-flask. Detection of reaction intermediates were carried to get an insight into the reaction pathway.

Iron-Catalyzed Cross-Coupling of Bis-(aryl)manganese Nucleophiles with Alkenyl Halides: Optimization and mechanistic investigations

Various substituted bis-(aryl)manganese species were prepared from aryl bromides by one-pot insertion of magnesium turnings in the presence of LiCl and in situ trans-metalation with MnCl2 in THF at ?5 ?C within 2 h. These bis-(aryl)manganese reagents undergo smooth iron-catalyzed cross-couplings using 10 mol% Fe(acac)3 with various functionalized alkenyl iodides and bromides in 1 h at 25 ?C. The aryl-alkenyl cross-coupling reaction mechanism was thoroughly investigated through paramagnetic 1H-NMR, which identified the key role of tris-coordinated ate-iron(II) species in the catalytic process.