142697-70-9

Basic information

• Product Name: 2-Cyclopenten-1-ol,4-amino-,acetate(ester),(1R-trans)-(9CI)
• Synonyms: 2-Cyclopenten-1-ol,4-amino-,acetate(ester),(1R-trans)-(9CI)
• CAS NO: 142697-70-9
• Molecular Formula: C7H11NO2
• Molecular Weight: 141.17
• Product Categories: VARIOUSAMINE
• Mol File: 142697-70-9.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Cyclopenten-1-ol,4-amino-,acetate(ester),(1R-trans)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclopenten-1-ol,4-amino-,acetate(ester),(1R-trans)-(9CI)(142697-70-9)
• EPA Substance Registry System: 2-Cyclopenten-1-ol,4-amino-,acetate(ester),(1R-trans)-(9CI)(142697-70-9)

Safety Data

• Hazardous Substances Data: 142697-70-9(Hazardous Substances Data)

Upstream product

• 60410-16-4 (1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate 
• 142633-87-2 (1R,4R)-trans-1-acetoxy-4-(N-phthalimidoamino)-2-cyclopentene 

Downstream Products

• 142633-89-4 (1R,4R)-trans-1-hydroxy-4-<<(tert-butyloxy)carbonyl>amino>-2-cyclopentene 

Relevant articles and documents

Novel practical deprotection of N-Boc compounds using fluorinated alcohols

The thermolytic deprotection of N-Boc compounds was accomplished using TFE (2,2,2-trifluoroethanol) or HFIP (hexafluoroisopropanol) as solvents. Even though the cleavage of the t-butylcarbamate (Boc) group can be achieved at solvent reflux temperature, the deprotection process was significantly accelerated under microwave-assisted conditions. The practicality of this methodology was demonstrated on alkyl, aryl, and heteroaromatic N-Boc-amines. Copyright Taylor & Francis Group, LLC.