219506-75-9

Basic information

• Product Name: BENZYL 2-ETHYL ACRYLATE 99
• Synonyms: BENZYL 2-ETHYL ACRYLATE 99;Butanoic acid, 2-Methylene-, phenylMethyl ester
• CAS NO: 219506-75-9
• Molecular Formula: C₁₂H₁₄O₂
• Molecular Weight: 190.23836
• Mol File: 219506-75-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: BENZYL 2-ETHYL ACRYLATE 99(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL 2-ETHYL ACRYLATE 99(219506-75-9)
• EPA Substance Registry System: BENZYL 2-ETHYL ACRYLATE 99(219506-75-9)

Safety Data

• Hazard Codes: Xi,N
• Statements: 36/37/38-51/53
• Safety Statements: 26-28-61
• RIDADR: UN 3082 9/PG 3
• WGK Germany: 2
• Hazardous Substances Data: 219506-75-9(Hazardous Substances Data)

Upstream product

• 51951-27-0 2-isopropoxyisoindoline-1,3-dione 
• 89295-32-9 2-(ethoxycarbonyl)prop-2-en-1-yl phenyl sulfone 
• 4390-96-9 2-ethylacryloyl chloride 
• 100-51-6 benzyl alcohol 
• 3586-58-1 2-methylenebutyric acid 

Downstream Products

• 219506-81-7 benzyl (2S)-2-(N-4-nitrobenzyloxycarbonylamino)-4-{[(2R,S)-2-(benzyloxycarbonyl)butyl]-(R,S)-N-(o-xylylenephosphoryl)-sulfonimidoyl}butanoate 
• 219506-80-6 benzyl (2S)-4-[(2R,S)-2-(benzyloxycarbonyl)butyl-(R,S)-sulfonimidoyl]-2-(N-4-nitrobenzyloxycarbonylamino)butanoate 
• 219506-79-3 (S)-4-(2-Benzyloxycarbonyl-butane-1-sulfinyl)-2-(4-nitro-benzyloxycarbonylamino)-butyric acid benzyl ester 
• 219506-77-1 (S)-4-(2-Benzyloxycarbonyl-butylsulfanyl)-2-(4-nitro-benzyloxycarbonylamino)-butyric acid benzyl ester 

Relevant articles and documents

Alkylation of Allyl/Alkenyl Sulfones by Deoxygenation of Alkoxyl Radicals

A challenging deoxygenation of alkoxyl radicals from readily accessible alcohol derivatives was developed, affording facile synthesis of functionalized alkenes with good functional group tolerance under mild reaction conditions. Because alkoxyl radicals can easily undergo β-fragmentations or hydrogen abstractions, this new strategy for deoxygenation of alkoxyl radicals is highly valuable. Moreover, mechanistic studies revealed that the electron-neutral phosphine acts as the deoxygenation reagent.