146831-96-1

Basic information

• Product Name: 1,5-di[2-(2'-carboxyhexadecyloxy)phenoxy]-3-oxapentane
• Synonyms: 1,5-di[2-(2'-carboxyhexadecyloxy)phenoxy]-3-oxapentane
• CAS NO: 146831-96-1
• Molecular Weight: 799.142
• Mol File: 146831-96-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,5-di[2-(2'-carboxyhexadecyloxy)phenoxy]-3-oxapentane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-di[2-(2'-carboxyhexadecyloxy)phenoxy]-3-oxapentane(146831-96-1)
• EPA Substance Registry System: 1,5-di[2-(2'-carboxyhexadecyloxy)phenoxy]-3-oxapentane(146831-96-1)

Safety Data

• Hazardous Substances Data: 146831-96-1(Hazardous Substances Data)

Upstream product

• 23116-94-1 bis(2-hydroxyphenoxyethyl)ether 
• 18263-25-7 2-bromopalmitic acid 

Downstream Products

• 154813-64-6 1,5-di[2-(2'-O-benzyl hydroxamatohexadecyloxy)phenoxy]-3-oxapentane 
• 154813-63-5 2-[2-(2-{2-[2-(1-chlorocarbonyl-pentadecyloxy)-phenoxy]-ethoxy}-ethoxy)-phenoxy]-hexadecanoyl chloride 

Relevant articles and documents

Synthesis of new lipophilic acyclic di-ionizable polyethers, bis(crown ethers) and macrocyclic diamides

A series of new lipophilic acyclic polyethers containing two carboxylic or hydroxamic acid groups have been prepared. From lipophilic acyclic polyether dicarboxylic acids 2, 9 and 13, the bis(crown ethers) 20-25 were synthesized. From lipophilic acyclic polyether dicarboxylic acids 10-12 and 14, the new macrocyclic diamides 26-32 were prepared in high yields without the use of high dilution techniques or template effects.

Separation of 90Y from 90Sr by solvent extraction with ionizable crown ethers

sym-Dibenzo-16-crown-5-oxyacetic acid and its analogues are selective for the extraction of Y3+ over Sr2+ from aqueous solutions into chloroform. The selectivity and the pH range of extraction are influenced by the structure of the l