23089-58-9

Basic information

• Product Name: 3-(Acetylamino)-2,3,6-trideoxy-D-arabino-hexopyranose
• Synonyms: 3-(Acetylamino)-2,3,6-trideoxy-D-arabino-hexopyranose
• CAS NO: 23089-58-9
• Molecular Formula: C₈H₁₅NO₄
• Molecular Weight: 189.209
• Mol File: 23089-58-9.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(Acetylamino)-2,3,6-trideoxy-D-arabino-hexopyranose(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Acetylamino)-2,3,6-trideoxy-D-arabino-hexopyranose(23089-58-9)
• EPA Substance Registry System: 3-(Acetylamino)-2,3,6-trideoxy-D-arabino-hexopyranose(23089-58-9)

Safety Data

• Hazardous Substances Data: 23089-58-9(Hazardous Substances Data)

Upstream product

• 81348-15-4 methyl 3-acetamido-2,3,6-trideoxy-4-O-(2-methoxyethoxymethyl)-α-L-ribo-hexopyranoside 
• 84765-87-7 methyl 3-acetamido-2,3,6-trideoxy-4-O-(methoxymethyl)-α-L-ribo-hexopyranoside 
• 61199-73-3 methyl 2,3-O-benzylidene-6-deoxy-α-L-mannopyranoside 
• 81348-07-4 methyl 2,6-dideoxy-4-O-(2-methoxyethoxymethyl)-α-L-erythro-hexopyranosid-3-ulose 
• 84765-85-5 methyl 2,6-dideoxy-4-O-(2-methoxyethoxymethyl)-α-L-erythro-hexopyranosid-3-ulose oxime 
• 1002757-17-6 methyl 2,3-O-benzylidene-6-deoxy-4-O-(methoxymethyl)-α-L-mannopyranoside 
• 1002757-16-5 methyl 2,3-O-benzylidene-6-deoxy-4-O-(2-methoxyethoxymethyl)-α-L-mannopyranoside 
• 81348-08-5 methyl 2,6-dideoxy-4-O-(methoxymethyl)-α-L-erythro-hexopyranosid-3-ulose 
• 84765-86-6 methyl 2,6-dideoxy-4-O-(methoxymethyl)-α-L-erythro-hexopyranosid-3-ulose oxime 
• 23089-57-8 methyl β-N-acetylacosaminide 
• 73938-74-6 Viridopentaose A 
• 73938-73-5 Viridopentaose C 
• 73793-33-6 Viridopentaose B 
• 129094-27-5 N-[(R)-3,3-Dimethoxy-1-((4S,5S)-2,2,5-trimethyl-[1,3]dioxolan-4-yl)-propyl]-acetamide 

Downstream Products

• 6605-27-2 methyl 3-acetamido-2,3,6-trideoxy-arabino-β-D,L-hexopyranoside 
• 6605-27-2 methyl 3-acetamido-2,3,6-trideoxy-arabino-α-D,L-hexopyranoside 
• 81227-30-7 3-acetamido-1-O-acetyl-2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-D-ribo-hexofuranose 
• 81227-42-1 methyl 2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-3-(p-nitrobenzoylacetamido)-α-D-ribo-hexofuranoside 
• 81227-28-3 methyl 3-acetamido-2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-α-D-ribo-hexofuranoside 
• 81227-31-8 methyl 3-acetamido-2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-β-D-ribo-hexofuranoside 
• 81227-36-3 methyl 2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-3-(trifluoroacetamido)-β-D-ribo-hexofuranoside 
• 81227-33-0 methyl 2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-3-(trifluoroacetamido)-α-D-ribo-hexofuranoside 
• 81227-34-1 1-O-acetyl-2,3,6-trideoxy-5-O-(p-nitrobenzoyl)-3-(trifluoroacetamido)-D-ribo-hexofuranose 

Relevant articles and documents

STRUCTURAL INVESTIGATION OF AN ANTIBIOTIC SPORAVIRIDIN IV. STRUCTURAL REVISION OF VIRIDOPENTAOSES

Structures of viridopentaose A, B and C are revised as 4A, 4B and 4C, respectively, by 1H-NMR (360 MHz) spectra and chemical degradations.

Syntheses of spacer-linked neodisaccharides derived from L-Daunosamine

The preparation of novel head-to-head spacer-linked bisdaunosamine homodimers 8, 15 and 18 is described. The synthesis is achieved by double glycosylation of monosilylated 1,4-butanediol 9 using silyl glycoside 5 as glycosyl donor. Alternatively, olefin metathesis of allyl glycosides α-11 and particularly of α-12 constitutes a second route toward 8 and its unsaturated derivative 15 while non symmetrical dimer 18 has been obtained by cross metathesis of allyl glycosides 11 and 12.

CONVENIENT SYNTHESYS OF L-DAUNOSAMINE AND L-ACOSAMINE

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THE SYNTHESIS OF 3-ACETAMIDO-2,3,5,6-TETRADEOXY-5-FLUORO-D,L-ribo-HEXOFURANOSE BY THE DIRECT FLUORINATION OF METHYL 3-ACETAMIDO-2,3,6-TRIDEOXY-D,L-arabino-HEXOPYRANOSIDE (METHYL N-ACETYL-D,L-ACOSAMINIDE)

3-Acetamido-2,3,5,6-tetradeoxy-5-fluoro-D,L-ribo-hexofuranose was synthesized by direct, fluorinative dehydroxylation of methyl 3-acetamido-2,3,6-trideoxy-D,L-arabino-hexopyranoside with sulfur tetrafluoride-hydrogen fluoride.The furanose form and the ribo configuration, indicated by 13C- and 1H-n. m. r. spectroscopy, respectively, were confirmed by a single-crystal, X-ray diffraction study.