1383543-85-8

Basic information

• Product Name: 4-{4-[14-(11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-oxycarbonylamino)-4-oxo-6,9,12-trioxa-3-azatetradec-2-yl]-2-methoxy-5-nitrophenoxy}butanoic acid methyl ester
• CAS NO: 1383543-85-8
• Molecular Weight: 747.799
• Mol File: 1383543-85-8.mol

Chemical Properties

• CAS DataBase Reference: 4-{4-[14-(11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-oxycarbonylamino)-4-oxo-6,9,12-trioxa-3-azatetradec-2-yl]-2-methoxy-5-nitrophenoxy}butanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-{4-[14-(11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-oxycarbonylamino)-4-oxo-6,9,12-trioxa-3-azatetradec-2-yl]-2-methoxy-5-nitrophenoxy}butanoic acid methyl ester(1383543-85-8)
• EPA Substance Registry System: 4-{4-[14-(11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-oxycarbonylamino)-4-oxo-6,9,12-trioxa-3-azatetradec-2-yl]-2-methoxy-5-nitrophenoxy}butanoic acid methyl ester(1383543-85-8)

Safety Data

• Hazardous Substances Data: 1383543-85-8(Hazardous Substances Data)

Upstream product

• 462100-06-7 2-[2-[2-(2-[[(tert-butoxy)carbonyl]amino]ethoxy)ethoxy]ethoxyl]acetic acid 
• 162827-96-5 methyl 4-(2-methoxy-5-nitro-4-(1-trifluoroacetamido-ethyl)phenoxy)butanoate 
• 1383543-83-6 4-[2-methoxy-5-nitro-4-(1-aminoethyl)phenoxy]butanoic acid methyl ester hydrochloride 
• 1146195-73-4 methyl 2,2-dimethyl-4-oxo-3,8,11,14-tetraoxa-5-azahexadecan-16-oate 
• 1027338-09-5 11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-yl carbonic acid 4-nitrophenyl ester 

Downstream Products

• 1393183-02-2 4-{4-[14-(11,12-didehydro-5,6-dihydrodibenzo[a,e]cycloocten-5-oxycarbonylamino)-4-oxo-6,9,12-trioxa-3-azatetradec-2-yl]-2-methoxy-5-nitrophenoxy}butanoic acid 4-nitophenyl ester 

Relevant articles and documents

Strategy for catch and release of azide-tagged biomolecules utilizing a photolabile strained alkyne construct

A photolabile o-nitrobenzyl linker-cyclooctyne conjugate was prepared, immobilized on poly(methacrylate) beads and utilized as a trap for azide-functionalized compounds. These could be released by 365 nm UV light irradiation in high yield and purity. The reagent-free and time economic catch and release protocol was deemed useful for chemical proteomics applications.