201005-58-5

Basic information

• Product Name: R-(+)-(2E)-N-(1-hydroxybutan-2-yl)-3-phenylprop-2-enamide
• Synonyms: R-(+)-(2E)-N-(1-hydroxybutan-2-yl)-3-phenylprop-2-enamide
• CAS NO: 201005-58-5
• Molecular Weight: 219.283
• Mol File: 201005-58-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: R-(+)-(2E)-N-(1-hydroxybutan-2-yl)-3-phenylprop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: R-(+)-(2E)-N-(1-hydroxybutan-2-yl)-3-phenylprop-2-enamide(201005-58-5)
• EPA Substance Registry System: R-(+)-(2E)-N-(1-hydroxybutan-2-yl)-3-phenylprop-2-enamide(201005-58-5)

Safety Data

• Hazardous Substances Data: 201005-58-5(Hazardous Substances Data)

Upstream product

• 96-20-8 2-aminobutanol 
• 102-92-1 Cinnamoyl chloride 
• 5856-63-3 (2R)-2-aminobutan-1-ol 

Downstream Products

• 201005-62-1 (4R,E)-4-ethyl-2-(2-phenylethenyl)-4,5-dihydro-1,3-oxazole 

Relevant articles and documents

Anticonvulsant Activity of Enantiomeric N-trans-Cinnamoyl Derivatives of 2-Aminopropan-1-ols and 2-Aminobutan-1-ols

Epilepsy, one of the most frequent neurological disorders, is still insufficiently treated in about 30% of patients. As a consequence, identification of novel anticonvulsant agents is an important issue in medicinal chemistry. In the present article we re

Asymmetric hetero-Diels-Alder reactions of alkenyldihydrooxazoles. Synthesis of oxazolo[3,2-c]pyrimidines and related compounds

Alkenyldihydrooxazoles undergo a highly diastereoselective formal aza-Diels-Alder reaction with aryl and arenesulfonyl isocyanates to give oxazolo[3,2-c]pyrimidines. Depending on the substitution pattern of the alkenyldihydrooxazole, these compounds may then undergo addition of a second equivalent of the isocyanate to give either tetrahydrooxazoIo[3,2-c]pyrimidine-8-carboxamides or octahydroazeto[2,3-7]oxazolo[3,2c]pyrimidines. The second addition is sensitive to steric and electronic factors, and can be prevented in some cases. The Royal Society of Chemistry 1999.