158573-62-7

Upstream product

• 4282-40-0 1-Iodoheptane 
• 13036-02-7 Dimethyl 5-hydroxyisophthalate 
• 618-83-7 5-Hydroxyisophthalic acid 

Downstream Products

• 129648-65-3 5-heptyloxy-1,3-benzenedicarboxylic acid 
• 158648-22-7 (5S,15R)-5,15-Bis-benzyloxymethyl-21-heptyloxy-7,10,13-trioxa-4,16-diaza-bicyclo[17.3.1]tricosa-1⁽²²⁾,19⁽²³⁾,20-triene-3,6,14,17-tetraone 
• 158573-55-8 (5S,15S)-5,15-Bis-benzyloxymethyl-21-heptyloxy-7,10,13-trioxa-4,16-diaza-bicyclo[17.3.1]tricosa-1⁽²²⁾,19⁽²³⁾,20-triene-3,6,14,17-tetraone 
• 158573-66-1 1,3-bis(carboxymethyl)-5-(heptyloxy)benzene 
• 158573-65-0 1,3-bis(cyanomethyl)-5-(heptyloxy)benzene 
• 158573-64-9 1,3-bis(chloromethyl)-5-(heptyloxy)benzene 
• 158573-63-8 1,3-bis(hydroxymethyl)-5-(heptyloxy)benzene 

Relevant academic research and scientific papers

Two-Dimensional versus Three-Dimensional Self-Assembly of a Series of 5-Alkoxyisophthalic Acids

Physisorbed self-assembled monolayers (SAMs) have been suggested as potential models for three-dimensional (3D) crystallization. This work studies the effect of altering the chain length of 5-alkoxyisophthalic acid (CnISA) on self-assembled mor

Syntheses of amino acid based phosphodiester linkage-containing cryptands as well as diphosphorylated macrocycles

The syntheses of two amino acid based phosphodiester linkage-containing cryptands (30 and 44) as well as diphosphorylated macrocycles (28, 29, 32 and 33) are described. Boc-L-Ser(Bn)-OH and/or Boc-D-Ser(Bn)-OH were used for the construction of the precursors for the diphosphitylation and macrocyclization by phosphitylation. The carboxylic acid groups were connected with a diethylene glyeol unit and the amino functionalities were linked using (ethylenedioxy)diacetic acid, oxydiacetic acid, or an isophthalic acid derivative. The LD-cryptands 30 and 44 were obtained after phosphitylation of the precursors 12 and 16, respectively, containing (ethylenedioxy)acetic acid or an isophthalic acid derivative as a bottom-spacer, using 4-chlorobenzyl phosphorodichlorodite followed by oxidation and hydrogenolysis. Phosphitylation of the precursors containing (ethylenedioxy)acetic acid or oxydiacetic acid as bottom-spacers 11-14, using bis(4-chlorobenzyl) N,N-diisopropylphosphoramidite and subsequent oxidation resulted in the corresponding diphosphorylated macrocycles 28, 29, 32, and 33.