51816-21-8

Basic information

• Product Name: 2-(2-phenylethyl)-Δ²-oxazoline
• Synonyms: 2-(2-phenylethyl)-Δ²-oxazoline
• CAS NO: 51816-21-8
• Molecular Weight: 175.23
• Mol File: 51816-21-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(2-phenylethyl)-Δ²-oxazoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-phenylethyl)-Δ²-oxazoline(51816-21-8)
• EPA Substance Registry System: 2-(2-phenylethyl)-Δ²-oxazoline(51816-21-8)

Safety Data

• Hazardous Substances Data: 51816-21-8(Hazardous Substances Data)

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 141-43-5 ethanolamine 
• 349431-92-1 C₁₁H₁₄BrNO 
• 645-59-0 dihydrocinnamonitrile 
• 51816-46-7 N‐(2‐hydroxyethyl)‐3‐phenylpropanamide 
• 3234-51-3 1,1-dibromo-2-phenylcyclopropane 
• 51816-10-5 N-(2-chloro-ethyl)-3-phenyl-propionamide 

Downstream Products

• 31508-44-8 2-phenylpropionic acid methyl ester 
• 103-25-3 3-phenylpropanoic acid methyl ester 

Relevant articles and documents

An efficient oxidative conversion of aldehydes into 2-substituted 2-oxazolines using 1,3-diiodo-5,5-dimethylhydantoin

Various aromatic and aliphatic aldehydes were converted into the corresponding 2-aryl and 2-alkyl-2-oxazolines, respectively, in good to high yields by reaction with 2-aminoethanol and 1,3-diiodo-5,5-dimethylhydantoin. Moreover, chiral bis-2-oxazolines, which can be used as chiral ligands in asymmetric synthesis, could be also prepared in moderate yields by the reaction of dialdehydes with (R)-(-)-2-phenylglycinol under the same conditions. Georg Thieme Verlag Stuttgart.

Convenient one-pot synthesis of 2-oxazolines from carboxylic acids

Simple one-pot methods for preparation of 2-oxazolines have been developed using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). Treatment of a mixture of carboxylic acids and 2-haloethylammonium salts with DMT-MM in methanol

PRODUCTION OF 2-PHENYL-1-CYCLOPROPANONE ACETALS FROM 2,2-DIBROMO-1-PHENYLCYCLOPROPANE

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