6847-14-9

Basic information

• Product Name: N-benzoyl-β-D-glucosamine
• Synonyms: N-benzoyl-β-D-glucosamine
• CAS NO: 6847-14-9
• Molecular Weight: 283.281
• Mol File: 6847-14-9.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: N-benzoyl-β-D-glucosamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzoyl-β-D-glucosamine(6847-14-9)
• EPA Substance Registry System: N-benzoyl-β-D-glucosamine(6847-14-9)

Safety Data

• Hazardous Substances Data: 6847-14-9(Hazardous Substances Data)

Upstream product

• 959-22-8 p-nitrophenylbenzoate 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 93-97-0 benzoic acid anhydride 
• 65-85-0 benzoic acid 
• 98-88-4 benzoyl chloride 
• 14257-69-3 glucosamine 
• 90-76-6 2-deoxy-2-amino glucose 

Downstream Products

• 4710-90-1 Benzyl-N-benzoyl-D-glucosaminid 
• 19949-65-6 5'.6'-O-Isopropyliden-2-phenyl-α-D-glucofuranol<2'.1':4.5>-Δ²-oxazolin 
• 14086-92-1 Ac₄Glc₂Bz 
• 907573-38-0 C₁₃H₁₇NO₇ 
• 66025-50-1 2-Phenyl-4,5-(3-O-(L-1-carboxy-propyl)-5,6-isopropyliden-D-glucofurano)-Δ²-oxazolin 
• 66025-50-1 2-Phenyl-4,5-(3-O-(D-1-carboxy-propyl)-5,6-isopropyliden-D-glucofurano)-Δ²-oxazolin 
• 66025-52-3 2-Phenyl-4,5-(5,6-isopropyliden-3-O-carboxymethyl-D-glucofurano)-Δ²-oxazolin 
• 98762-83-5 2-Phenyl-4,5-(3-O-carbamylmethyl-5,6-isopropyliden-D-glucofurano)-Δ²-oxazolin 
• 102874-34-0 [(4S,5R)-5-((E)-Pentadec-1-enyl)-2-phenyl-4,5-dihydro-oxazol-4-yl]-methanol 
• 911-74-0 3-O-benzoylsphingosine hydrochloride 
• 144150-66-3 2-phenyl-(2,3-dideoxy-4,6-O-ethylidene-D-allopyranoso)<2,3-d>-4,5 dihydrooxazole 
• 144150-67-4 (2R,4R,5R)-4-((4S,5S)-4-Hydroxymethyl-2-phenyl-4,5-dihydro-oxazol-5-yl)-2-methyl-[1,3]dioxan-5-ol 
• 144150-68-5 (3aS,6aS)-2-Phenyl-3a,4,6,6a-tetrahydro-furo[3,4-d]oxazol-6-ol 
• 4201-55-2 3-O-benzoyl-ceramide 

Relevant articles and documents

New Synthetic Methods and Reagents for Complex Carbohydrates. II. Synthesis of 2-Acylamino-2-deoxy-D-glucopyranose Derivatives by Dimethylphosphinothioic Anhydride Method

Dimethylphosphinothioic (Mpt) mixed anhydrides of carboxylic acids were found to be useful for N-acylation of 2-amino-2-deoxy-D-glucopyranose derivatives without protecting the hydroxyl functions.By this method, N-acylation of 2-amino-2-deoxy-D-glucopyran

Synthesis of β-acylamino furans from glucosamine

A facile method for the synthesis of a series of novel β-acylamino furans stating from renewable monosaccharide was achieved. Glucosamine hydrochloride was selectively N-acylated with acyl chlorides in methanol/triethylamine to yield N-acyl-d-glucosamines, which were subsequently converted into β-acylamino furans through dehydration and cyclization under microwave irradiation.

A chemoenzymatic route to N-acetylglucosamine-1-phosphate analogues: Substrate specificity investigations of N-acetylhexosamine 1-kinase

Reports an efficient chemoenzymatic production of an N-acetylhexosamine 1-phophate analogues library by N-acetylhexosamine 1-kinase (NahK) and describes the respective substrate specificity on this enzyme.