727428-90-2

Basic information

• Product Name: 3-Oxabicyclo[3.2.0]heptane-2-carboxylicacid,methylester,(1R,2R,5S)-(9CI)
• Synonyms: 3-Oxabicyclo[3.2.0]heptane-2-carboxylicacid,methylester,(1R,2R,5S)-(9CI)
• CAS NO: 727428-90-2
• Molecular Formula: C8H12O3
• Molecular Weight: 0
• Product Categories: CARBOXYLICESTER
• Mol File: 727428-90-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Oxabicyclo[3.2.0]heptane-2-carboxylicacid,methylester,(1R,2R,5S)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Oxabicyclo[3.2.0]heptane-2-carboxylicacid,methylester,(1R,2R,5S)-(9CI)(727428-90-2)
• EPA Substance Registry System: 3-Oxabicyclo[3.2.0]heptane-2-carboxylicacid,methylester,(1R,2R,5S)-(9CI)(727428-90-2)

Safety Data

• Hazardous Substances Data: 727428-90-2(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 727428-85-5 (R)-(1S,2S,5R)-2-(3-Oxa-bicyclo[3.2.0]hept-2-yl)-1,4-dioxa-spiro[4.5]decane 
• 954406-21-4 (R)-2-(1-Allyloxy-allyl)-1,4-dioxa-spiro[4.5]decane 
• 727428-84-4 (2R)-2-[(1R,2R,5S)-3-oxabicyclo[3.2.0]hept-2-yl]-1,4-dioxa-spiro[4.5]decane 

Relevant articles and documents

Asymmetric induction in copper (I)-catalyzed intramolecular [2 + 2] photocycloaddition: Synthesis of enantiopure cyclobutane derivatives

A simple approach for asymmetric induction in copper (I)-catalyzed intramolecular [2 + 2] photocycloaddition of 1,6-dienes, where asymmetric catalysis or chiral auxiliaries have been inefficient, has been developed using the concept of chirality transfer

Copper(I)-catalyzed intramolecular asymmetric [2 + 2] photocycloaddition. Synthesis of both enantiomers of cyclobutane derivatives

Equation presented. A simple approach for asymmetric induction in Cu(I)-catalyzed [2 + 2] photocycloaddition, where asymmetric catalysts or chiral auxiliaries were inefficient, has been developed using the concept of chirality transfer from the readily av