1422064-26-3

Basic information

• Product Name: 1-(bromomethyl)-4-(4-methoxybutoxy)benzene
• Synonyms: 1-(bromomethyl)-4-(4-methoxybutoxy)benzene
• CAS NO: 1422064-26-3
• Molecular Weight: 273.17
• Mol File: 1422064-26-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(bromomethyl)-4-(4-methoxybutoxy)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(bromomethyl)-4-(4-methoxybutoxy)benzene(1422064-26-3)
• EPA Substance Registry System: 1-(bromomethyl)-4-(4-methoxybutoxy)benzene(1422064-26-3)

Safety Data

• Hazardous Substances Data: 1422064-26-3(Hazardous Substances Data)

Upstream product

• 111-32-0 4-methoxybutanol 
• 4457-67-4 4-Methoxy-1-bromobutane 
• 1422064-25-2 [4-(4-methoxybutoxy)phenyl]methanol 

Downstream Products

• 1422064-31-0 methyl 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolinate 
• 1422064-40-1 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-L-histidine 
• 1422064-34-3 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-proline 
• 1422064-37-6 benzyl 1-[4-(4-methoxybutoxy)benzyl]-5-oxo-L-prolyl-3-trityl-L-histidinate 

Relevant articles and documents

Synthesis of new optically active 2-pyrrolidinones

A new class of optically active 2-pyrrolidinones was synthesized, starting from S-pyroglutamic acid, a well known natural chiral synthon. The synthetic design followed led to the insertion of various substituents at positions 1 and 5 of the 2-pyrrolidinone ring, including the imidazole moiety. Some of them possess two or three stereogenic centers, the configuration of which was retained under the mild conditions used. The new compounds also carry an imidazole moiety, which, along with the 2-pyrrolidinone template, may prove pivotal to several biological processes.