169267-67-8

Basic information

• Product Name: 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid
• Synonyms: 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid
• CAS NO: 169267-67-8
• Molecular Weight: 447.531
• Mol File: 169267-67-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid(169267-67-8)
• EPA Substance Registry System: 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid(169267-67-8)

Safety Data

• Hazardous Substances Data: 169267-67-8(Hazardous Substances Data)

Upstream product

• 767-00-0 4-cyanophenol 
• 873-75-6 4-bromobenzenemethanol 
• 188051-26-5 Methyl-1-tert-butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylate 
• 41841-16-1 (4-bromo-phenyl)-acetic acid methyl ester 
• 169267-65-6 1-Bromo-8-tert-butoxycarbonylamino-7-oxo-3-oxa-6-aza-1(1,4),4(1,4)-dibenzaoctaphane 
• 155720-37-9 11-Bromo-5-amino-3-oxa-1(1,4),4(1,4)-dibenzapentaphane 
• 155720-38-0 11-Bromo-4-cyano-3-oxa-1(1,4),4(1,4)-dibenzatetraphane 

Downstream Products

• 169267-70-3 N-{1-[6-(2-{4'-[4-(tert-Butoxycarbonylamino-methyl)-phenoxymethyl]-biphenyl-4-yl}-acetylamino)-pyridin-2-ylcarbamoyl]-2-phenyl-ethyl}-succinamic acid allyl ester 
• 188051-31-2 N-{(S)-1-[6-(2-{4'-[4-(tert-Butoxycarbonylamino-methyl)-phenoxymethyl]-biphenyl-4-yl}-acetylamino)-pyridin-2-ylcarbamoyl]-2-phenyl-ethyl}-succinamic acid allyl ester 
• 188051-29-8 1-tert-Butoxycarbonylamino-3-oxa-2(1,4),5(1,4),6(1,4)-tribenzaheptaphane-7-carboxylic acid fluoride 

Relevant articles and documents

Synthesis and binding properties of a macrocyclic peptide receptor

Macrocyclic receptor 1 has been synthesised, as a racemate and as a single enantiomer, utilising a Stille coupling for the formation of the biphenyl portion and a macrolactamisation as the final step. The binding properties for the racemic and the homochi

Synthesis and binding properties of peptide receptor

Macrocyclic receptor 2, with an amidopyridine unit as the binding site for carboxylic acid functionally and amide functionality to provide additional hydrogen bonding sites, has been synthesised. Preliminary binding studies with 2 and various peptidic gue