102039-77-0

Basic information

• Product Name: N,N'-diacetylchitobiosamine
• Synonyms: N,N'-diacetylchitobiosamine
• CAS NO: 102039-77-0
• Molecular Weight: 423.42
• Mol File: 102039-77-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N,N'-diacetylchitobiosamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-diacetylchitobiosamine(102039-77-0)
• EPA Substance Registry System: N,N'-diacetylchitobiosamine(102039-77-0)

Safety Data

• Hazardous Substances Data: 102039-77-0(Hazardous Substances Data)

Upstream product

• 29625-73-8 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1-N-(4-L-aspartoyl)-2-deoxy-β-D-glucopyranosylamine 

Downstream Products

• 1314582-97-2 2,2',2'',2'''-{{(2S)-3-{{4'-{[2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranosyl]carbamoyl}biphenyl-4-yl}amino}-3-oxopropane-1,2-diyl}dinitrilo}tetraacetic acid 
• 1332927-80-6 C₅₀H₈₀N₆O₂₀ 
• 1332927-81-7 C₃₄H₄₈N₆O₂₀ 
• 1198097-00-5 C₅₁H₇₂N₁₀O₁₇ 
• 1262658-50-3 C₆₇H₉₉N₁₃O₂₆ 
• 1262658-47-8 C₄₇H₇₁N₁₁O₂₄ 
• 14307-03-0 2-amino-2-deoxy-D-glucitol 
• 29625-73-8 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1-N-(4-L-aspartoyl)-2-deoxy-β-D-glucopyranosylamine 
• 174744-31-1 Ac-Glu-Asn(N,N'-diacetylchitobiosyl)-(Hmb)Ala-Ser-Lys-Ala-NH₂ 
• 908124-96-9 C₅₈H₉₀N₁₄O₂₃S 

Relevant articles and documents

A METHOD FOR REDUCTIVE CLEAVAGE OF N-GLYCOSYLAMIDE CARBOHYDRATE-PEPTIDE BOND

A new, mild method for the splitting of N-linked oligosaccharides from glycoproteins includes treatment of glycoproteins (ovomucoid, flavoprotein, ribonuclease B, hemagglutinin, or transferrin) with 2 M LiBH4 in 25 mM LiOH - 50 mM Li citrate - 70percent aqueous tert-butyl alcohol (5 h, 45 deg C), followed by hydrolysis of the resulting glycosylamine with aqueous acetic acid.The oligosaccharides formed were easily isolated by gel filtration and cation-exchange chromatography in 60-80 percent yields.The reaction was accompanied by the intense reductive cleavage of peptide bonds with formation of amino alcohols, but N-deacetylation of hexosamine was completely excluded.The optimal conditions of this reaction were chosen by use of a model glycopeptide, 2-acetamido-4-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-1-N-(4-L-aspartoyl)-2-deoxy-β-D-glucopyranosylamine