1346641-23-3

Basic information

• Product Name: 1-((benzyloxy)methyl)cyclopropane-1-carboxylic acid
• Synonyms: 1-((benzyloxy)methyl)cyclopropane-1-carboxylic acid
• CAS NO: 1346641-23-3
• Molecular Weight: 206.241
• Mol File: 1346641-23-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-((benzyloxy)methyl)cyclopropane-1-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((benzyloxy)methyl)cyclopropane-1-carboxylic acid(1346641-23-3)
• EPA Substance Registry System: 1-((benzyloxy)methyl)cyclopropane-1-carboxylic acid(1346641-23-3)

Safety Data

• Hazardous Substances Data: 1346641-23-3(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 88157-42-0 methyl 1-(hydroxymethyl)cyclopropane-1-carboxylate 
• 103-63-9 1-phenyl-2-bromoethane 
• 39590-81-3 [1-(hydroxymethyl)cyclopropyl]methanol 
• 177200-76-9 {1-[(benzyloxy)methyl]cyclopropyl}methanol 
• 17690-16-3 benzyl bromomethyl ether 
• 1346641-19-7 C₁₆H₂₂O₃ 

Downstream Products

• 1346641-07-3 1-((benzyloxy)methyl)-N-(4-cyano-2,3,5,6-tetrafluorophenyl)cyclopropanecarboxamide 

Relevant articles and documents

PD(II)-CATALYZED ENANTIOSELECTIVE C-H ARYLATION OF FREE CARBOXYLIC ACIDS

The invention includes procedures for stereoselective β-arylation of carboxylic acids having a β-carbon atom. For example, stereoselective arylation procedures include the following reactions: (I)

Pd(II)-Catalyzed Enantioselective C(sp3)-H Arylation of Free Carboxylic Acids

A monoprotected aminoethyl amine chiral ligand based on an ethylenediamine backbone was developed to achieve Pd-catalyzed enantioselective C(sp3)-H arylation of cyclopropanecarboxylic and 2-aminoisobutyric acids without using exogenous directing groups. This new chiral catalyst affords new disconnection for preparing diverse chiral carboxylic acids from simple starting materials that are complementary to the various ring forming approaches.