121481-90-1

Basic information

• Product Name: (+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine
• CAS NO: 121481-90-1
• Molecular Weight: 113.159
• Mol File: 121481-90-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine(121481-90-1)
• EPA Substance Registry System: (+/-)-cis-(4-hydroxymethyl)cyclopent-2-en-1-ylamine(121481-90-1)

Safety Data

• Hazardous Substances Data: 121481-90-1(Hazardous Substances Data)

Upstream product

• 132243-27-7 cis-4-hydroxymethyl-1-ureidocyclopent-2-ene 
• 132243-26-6 2-carbamoyl-2-azabicyclo<2.2.1>hept-5-en-3-one 
• 144534-63-4 anti-3-(benzyloxy)methyl-1,5-epoxycyclopentane 
• 144534-59-8 (3-cyclopenten-1-yl)methyl benzoate 
• 25125-21-7 4-(hydroxymethyl)cyclopentene 
• 162427-15-8 3-oxo-2-aza-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid tert-butyl ester 
• 49805-30-3 2-azabicyclo[2.2.1.]hept-5-en-3-one 
• 49805-30-3 racemic 2-azabicyclo[2.2.1]hept-5-en-3-one 
• 172720-97-7 (+/-)-tert-butyl (1RS,4SR)-4-(hydroxymethyl)cyclopent-2-enylcarbamate 
• 132243-25-5 2-(N-chloroacetylcarbamoyl)-2-azabicyclo<2.2.1>hept-5-en-3-one 

Downstream Products

• 172720-97-7 (+/-)-tert-butyl (1RS,4SR)-4-(hydroxymethyl)cyclopent-2-enylcarbamate 

Relevant articles and documents

Synthesis of novel N-cyclopentenyl-lactams using the Aubé reaction

A novel and convenient method utilizing the Aubé reaction to access a new class of compounds that are similar to carbocyclic nucleosides is reported. The azido alcohol derived from Vince lactam undergoes the Aubé reaction with various cyclic ketones to gi

Deamination of 9-(hydroxymethylated cycloalkyl)-9H-adenines (carbocyclic adenine nucleosides) by adenosine deaminase: Effect of high-pressure upon deamination rate and enantioselectivity

The deamination of eight kinds of racemic carbocyclic adenine nucleosides by adenosine deaminase under high-pressure (400 MPa) was examined and the result was compared with that obtained from the reaction under atmospheric pressure. The deamination of all

Synthesis of carbocyclic nucleosides from 2-azabicyclo[2.2.1]hept-5-en-3-ones: Sodium borohydride-mediated carbon-nitrogen bond cleavage of five- and six-membered lactams

Various carbocyclic ribofuranosyl nucleosides were stereoselectively synthesized through a small number of steps from 2-azabicyclo[2.2.1]hept-5-en-3-ones by the use of sodium borohydride-mediated C-N bond cleavage as a key step. Ready availability of a no