174775-01-0

Upstream product

• 2615-25-0 trans-1,4-cyclohexyldiamine 
• 175867-52-4 1-amino-4-(triphenylmethylamino)cyclohexane 
• 3114-70-3 trans-1,4-diaminocyclohexane 
• 845522-74-9 N-(4-amino-cyclohexyl)-2,2,2-trifluoro-acetamide 
• 5292-43-3 bromoacetic acid tert-butyl ester 
• 688044-38-4 N,N-di-tert-butylacetate-N'-trifluoroacetamide 1,4-trans-diaminocyclohexane 
• 174774-99-3 di-tert-butyl trans-[4-(triphenylmethylamino)cyclohexylamino]diacetate 

Downstream Products

• 259150-16-8 di-tert-butyl trans-[4-(5-amidinobenzofuran-2-carboxamido)cyclohexylamino]diacetate 
• 688044-40-8 {tert-butoxycarbonylmethyl-[4-({6-chloro-7-[1-(2-nitro-phenyl)-ethoxy]-2-oxo-2H-chromene-3-carbonyl}-amino)-cyclohexyl]-amino}-acetic acid tert-butyl ester 
• 688044-39-5 (tert-butoxycarbonylmethyl-{4-[(6-chloro-7-hydroxy-2-oxo-2H-chromene-3-carbonyl)-amino]-cyclohexyl}-amino)-acetic acid tert-butyl ester 
• 174774-32-4 di-tert-butyl trans-[4-[5-(benzyloxycarbonylamidino)benzofuran-2-carboxamido]cyclohexylamino]diacetate 

Relevant academic research and scientific papers

New Caged Coumarin Fluorophores with Extraordinary Uncaging Cross Sections Suitable for Biological Imaging Applications

Photocaged fluorescent molecules are important research tools for tracking molecular dynamics with high spatiotemporal resolution in biological systems. We have designed and synthesized a new class of caged coumarin fluorophores. These coumarin cages disp

Preparation and pharmacological evaluation of novel glycoprotein (Gp) IIb/IIIa antagonists. 2. Condensed heterocyclic derivatives

A novel series of platelet receptor glycoprotein (Gp) IIb/IIIa antagonists with condensed heterocycles as their basic core was synthesized. In an in vitro assay, trans-4-(5-amidinobenzofuran-2- carboxamido)cyclohexyl]oxyacetic acid 17e and trans-3-[4-(5-