156731-34-9

Basic information

• Product Name: 1-N-BOC-AMINO-2-CYCLOPENTENE
• Synonyms: 1-N-BOC-AMINO-2-CYCLOPENTENE;N-1-BOC-AMINO-2-CYCLOPENTENE;Carbamic acid, 2-cyclopenten-1-yl-, 1,1-dimethylethyl ester (9CI)
• CAS NO: 156731-34-9
• Molecular Formula: C10H17NO2
• Molecular Weight: 183.25
• Product Categories: N-BOC
• Mol File: 156731-34-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 268.9±20.0 °C(Predicted)
• Appearance: /
• Density: 1.01±0.1 g/cm3(Predicted)
• PKA: 12.22±0.20(Predicted)
• CAS DataBase Reference: 1-N-BOC-AMINO-2-CYCLOPENTENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-N-BOC-AMINO-2-CYCLOPENTENE(156731-34-9)
• EPA Substance Registry System: 1-N-BOC-AMINO-2-CYCLOPENTENE(156731-34-9)

Safety Data

• Hazardous Substances Data: 156731-34-9(Hazardous Substances Data)

Usage

General Description

1-N-BOC-AMINO-2-CYCLOPENTENE is a chemical compound with the molecular formula C10H17NO2. 1-N-BOC-AMINO-2-CYCLOPENTENE is categorized under organic compounds known as N-BOC amino acids and derivatives, which have a structure characterized by an amino acid substituted with a tert-butoxycarbonyl group at the N-terminal position. Its exact chemical structure is still subject to research and remains undefined within the scientific community, as more information concerning its properties and potential uses continues to be unearthed. Therefore, its applications are not fully identified. However, it is noteworthy that N-BOC amino acids and derivatives are important for peptide synthesis, which plays a crucial role in scientific sectors such as biology and medicinal chemistry.

Upstream product

• 142-29-0 cyclopentene 
• 24424-99-5 di-tert-butyl dicarbonate 
• 81097-48-5 N-tosyl-6-azabicyclo[3.1.0]hexane 
• 153789-12-9 N-(tert-butoxycarbonyl)-6-azabicyclo<3.1.0>hexane 
• 927837-71-6 C₉H₁₂Cl₃NO 
• 62019-06-1 (E)-2,6-heptadien-1-ol 
• 95514-62-8 (E)-ethyl hepta-2,6-dienoate 
• 100727-30-8 2-(cyclopent-2-en-1-yl)isoindoline-1,3-dione 

Downstream Products

• 657397-01-8 (2R)-(4-oxocyclopent-2-enyl)-carbamic acid tert-butyl ester 
• 189625-12-5 (+)-(1S,4R)-1-hydroxy-4-[(tert-butoxycarbonyl)amino]-2-cyclopentene 
• 34404-28-9 N-[(1,1-dimethylethoxy)carbonyl]-D-glutamic acid 

Relevant articles and documents

PCSK9 INHIBITORS AND METHODS OF USE THEREOF

The invention relates to a novel inhibitor pharmacophore of PCSK9 and heteroaryl compounds that bind the PCSK9 protein.

Asymmetric synthesis of cis-aminocyclopentenols, building blocks for medicinal chemistry

A highly efficient one-pot multistep process involving an asymmetric Pd(II)-catalyzed Overman rearrangement and a Ru(II)-catalyzed ring-closing metathesis reaction has been developed for the preparation of (R)- or (S)-aminocyclopenta-2-enes. The rapid strategy employed and the relatively mild conditions of the one-pot process allowed the multigram synthesis of the carbocycles in high enantiomeric excess (92% ee). The synthetic utility of these compounds was demonstrated by the stereoselective incorporation of hydroxyl groups, generating cis-4- and cis-5-aminocyclopenta-2-en-1-ols, important building blocks for medicinal chemistry.

Asymmetric Catalysis by Vitamin B12: The Isomerization of Achiral Aziridines to Optically Active Allylic Amines

Achiral N-acylaziridines are isomerized to optically active N-acyl-allylamines in ee's of up to 95percent by catalytic amounts of cob(I)alamin in MeOH.