191613-43-1

Basic information

• Product Name: {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid
• Synonyms: {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid
• CAS NO: 191613-43-1
• Molecular Weight: 582.562
• Mol File: 191613-43-1.mol

Chemical Properties

• CAS DataBase Reference: {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid(191613-43-1)
• EPA Substance Registry System: {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid(191613-43-1)

Safety Data

• Hazardous Substances Data: 191613-43-1(Hazardous Substances Data)

Upstream product

• 191613-42-0 {Benzyloxycarbonyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid tert-butyl ester 
• 64650-83-5 N-((2S,3R,4R,5R,6R)-2-Allyloxy-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl)-acetamide 
• 191613-39-5 Acetic acid (2R,3R,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(2-benzylamino-ethoxy)-tetrahydro-pyran-4-yl ester 
• 191613-40-8 {Benzyl-[2-((2S,3R,4R,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethyl]-amino}-acetic acid tert-butyl ester 
• 191613-41-9 [2-((2S,3R,4R,5R,6R)-4,5-Diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-yloxy)-ethylamino]-acetic acid tert-butyl ester 

Downstream Products

• 191613-48-6 C₄₄H₆₀N₄O₂₃ 
• 191613-46-4 C₄₈H₆₈N₄O₂₃ 

Relevant articles and documents

Oligomeric glycopeptidomimetics bearing the cancer related T(N)-antigen

α-O-Linked N-acelylgalactosamine clusters with 2, 3, 4, 6, and 8 repenting units were synthesized using a reiterative blockwise appronch and N-substituted oligoglycine peptoid backbones. Orthogonally protected glycopeptide 5 and 7 were used as key building blocks.