77745-30-3

Basic information

• Product Name: trans-4-Acetamidocyclopent-2-enemethyl Acetate
• CAS NO: 77745-30-3
• Molecular Weight: 197.234
• Mol File: 77745-30-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: trans-4-Acetamidocyclopent-2-enemethyl Acetate(CAS DataBase Reference)
• NIST Chemistry Reference: trans-4-Acetamidocyclopent-2-enemethyl Acetate(77745-30-3)
• EPA Substance Registry System: trans-4-Acetamidocyclopent-2-enemethyl Acetate(77745-30-3)

Safety Data

• Hazardous Substances Data: 77745-30-3(Hazardous Substances Data)

Upstream product

• 49805-30-3 2-azabicyclo[2.2.1.]hept-5-en-3-one 
• 77745-25-6 cis-4-amino-2-cyclopentenecarboxylic acid methyl ester hydrochloride 
• 77745-26-7 Methyl trans-4-Aminocyclopent-2-enecarboxylate Hydrochloride 
• 61865-62-1 cis-4-aminocyclopent-2-nene-1-carboxylic acid hydrochloride 
• 77745-29-0 trans-4-Aminocyclopent-2-enemethanol Hydrochloride 

Relevant articles and documents

Carbocyclic Sugar Amines: Synthesis and Stereochemistry of Racemic α- and β-Carbocyclic Ribofuranosylamine, Carbocyclic Lyxofuranosylamine, and Related Compounds

The facile and stereoselective synthesis of racemic carbocyclic β-ribofuranosylamine, carbocyclic β-lyxofuranosylamine, and related 2,3-cis-dihydroxy carbocyclic pentofuranosylamines is reported.In addition, the synthesis, isolation, and base-catalyzed epimerization of methyl cis-4-aminocyclopent-2-enecarboxylate are described.The epimerization at C(1) followed by stereoselective cis hydroxylation provides for the first time access to the racemic carbocyclic α-pentofuranosylamines.