22554-02-5

Basic information

• Product Name: ethyl N-(3-phenylprop-2-enyl)carbamate
• Synonyms: ethyl N-(3-phenylprop-2-enyl)carbamate
• CAS NO: 22554-02-5
• Molecular Weight: 205.257
• Mol File: 22554-02-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: ethyl N-(3-phenylprop-2-enyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl N-(3-phenylprop-2-enyl)carbamate(22554-02-5)
• EPA Substance Registry System: ethyl N-(3-phenylprop-2-enyl)carbamate(22554-02-5)

Safety Data

• Hazardous Substances Data: 22554-02-5(Hazardous Substances Data)

Upstream product

• 23583-01-9 O-carbethoxy-N-hydroxysuccinimide 
• 4360-51-4 cinnamylamine 
• 104-54-1 3-Phenylpropenol 
• 590-28-3 potassium cyanate 
• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 64-17-5 ethanol 
• 100-42-5 styrene 
• 67-68-5 dimethyl sulfoxide 
• 51-79-6 urethane 
• 57330-84-4 ethyl 3,4-dihydro-4-oxo-1(2H)-pyridinecarboxylate 
• 4392-24-9 Cinnamyl bromide 
• 1189-71-5 isocyanate de chlorosulfonyle 
• 1476-07-9 (E)-(3-ethoxy-1-propen-1-yl)benzene 
• 541-41-3 chloroformic acid ethyl ester 

Downstream Products

• 22665-13-0 1-phenylallyl methyl ether 
• 24808-73-9 (E)-(3-methoxyprop-1-en-1-yl)benzene 
• 22553-93-1 (E)-(3-diazoprop-1-en-1-yl)benzene 
• 107262-22-6 N-(2,3-Dibrom-3-phenylpropyl)-carbamidsaeureethylester 

Relevant articles and documents

Redox self-sufficient biocatalyst network for the amination of primary alcohols

Driving the machinery: A biocatalytic redox-neutral cascade for the preparation of terminal primary amines from primary alcohols at the expense of ammonia has been established in a one-pot one-step method (see picture). Applying this artificial biocatalyst network, long-chain 1,ω-alkanediols were converted into diamines, which are building blocks for polymers, in up to 99 % conversion. Copyright

Hydroxy Chalcogenide-Promoted Morita-Baylis-Hillman Alkylation Reaction: Intermolecular Applications with Alkyl Halides as Electrophiles

Hydroxysulfides acted as catalysts to promote the Morita-Baylis-Hillman alkylation reaction of cyclohexenones and dihydropyridinones. The procedure worked efficiently with a variety of halides as electrophiles. Side reactions were in competition with the

Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers

The stability order of various alkyl, allyl, and benzyl carbocations was investigated using the novel technique for comparing the stability of carbocations in solution developed by using a simple CSI reaction with various ethers. The p-methoxycinnamyl carbocation was the most stable in our reaction system and the next stable carbocation was the p-methoxybenzyl carbocation. The stability of the other carbocations decreased with methacryl, t-butyl, cinnamyl, acryl, benzyl, 2° and allyl carbocations in that order.