104684-78-8

Basic information

• Product Name: Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-((1R,2R,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-5-allyloxycarbonylamino-tetrahydro-pyran-4-yl ester
• Synonyms: Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-((1R,2R,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-5-allyloxycarbonylamino-tetrahydro-pyran-4-yl ester
• CAS NO: 104684-78-8
• Molecular Weight: 833.93
• Mol File: 104684-78-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-((1R,2R,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-5-allyloxycarbonylamino-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-((1R,2R,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-5-allyloxycarbonylamino-tetrahydro-pyran-4-yl ester(104684-78-8)
• EPA Substance Registry System: Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-6-((1R,2R,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-5-allyloxycarbonylamino-tetrahydro-pyran-4-yl ester(104684-78-8)

Safety Data

• Hazardous Substances Data: 104684-78-8(Hazardous Substances Data)

Upstream product

• 112929-24-5 1,3,4,6-tetra-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glucopyranose 
• 104655-87-0 3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glucopyranosyl bromide 
• 14131-62-5 D-glucosamine hydrochloride 
• 146934-02-3 2-deoxy-2-(allyloxycarbonylamino)-α-D-glucopyranoside 
• 112929-24-5 1,3,4,6-tetra-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranose 
• 102717-78-2 (2R,3R,4S)-5-Allyloxy-1,3,4-tris-benzyloxy-pentan-2-ol 
• 102717-78-2 1-O-allyl-2.3.5-tri-O-benzyl-D-ribitol 

Downstream Products

• 102717-83-9 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-((1R,2S,3S)-4-allyloxy-2,3-bis-benzyloxy-1-benzyloxymethyl-butoxy)-tetrahydro-pyran-4-yl ester 

Relevant articles and documents

N-Allyloxycarbonyl derivatives of D-glucosamine as promotors of 1,2-trans-glucosylation in Koenigs-Knorr reactions and in Lewis acid catalysed condensations

The use of suitably blocked D-glucosamine derivatives possessing the N-allyloxyxarbonyl protective group of the amino function represents potential new routes to 1,2-trans-glucosylations.Both 3,4,6-tri-O-acetyl-2-N-allyloxycarbonyl-2-amino-2-deoxy-α-D-glu