1141-01-1

Basic information

• Product Name: phenyl β-L-arabinopyranoside
• Synonyms: phenyl β-L-arabinopyranoside
• CAS NO: 1141-01-1
• Molecular Weight: 226.229
• Mol File: 1141-01-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: phenyl β-L-arabinopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl β-L-arabinopyranoside(1141-01-1)
• EPA Substance Registry System: phenyl β-L-arabinopyranoside(1141-01-1)

Safety Data

• Hazardous Substances Data: 1141-01-1(Hazardous Substances Data)

Upstream product

• 87-72-9 L-(+)-arabinose 
• 108-95-2 phenol 
• 17296-18-3 2,3,4-tri-O-chlorosulfonyl-β-D-xylopyranosyl chloride 
• 14227-90-8 2,3,4-tri-O-acetyl-α-L-arabinopyranosyl bromide 
• 1233-03-0 1,2,3,4-tetra-O-acetyl-α-L-arabinopyranose 
• 87903-70-6 phenyl 2,3,4-tri-O-acetyl-α-L-arabinopyranoside 

Downstream Products

• 103931-43-7 phenyl 3,4-dideoxy-β-D-glycero-pent-3-enopyranoside 2-acetate 
• 111476-61-0 phenyl 3,4-dideoxy-β-D-glycero-pent-3-enopyranoside 
• 111476-56-3 phenyl 4-deoxy-α-L-threo-pentopyranoside 2-acetate 
• 111476-55-2 phenyl 3-deoxy-β-L-threo-pentopyranoside 2-acetate 
• 104011-39-4 phenyl 3,4-dideoxy-β-D-glycero-pentopyranoside 
• 103931-42-6 Acetic acid (3aS,6S,7R,7aS)-6-phenoxy-2-thioxo-tetrahydro-[1,3]dioxolo[4,5-c]pyran-7-yl ester 
• 103931-39-1 (2S,3R,5R)-2-Phenoxy-tetrahydro-pyran-3,5-diol 
• 104118-44-7 (2S,3R,4S)-2-Phenoxy-tetrahydro-pyran-3,4-diol 
• 84380-09-6 phenyl 2,3,4-tri-O-acetyl-α-D-xylopyranoside 
• 5041-91-8 Phenyl 2,3,4-tri-O-acetyl-β-D-xylopyranoside 
• 103931-37-9 phenyl α-L-arabinopyranoside 3,4-thioncarbonate 
• 88087-53-0 Benzoic acid (2S,3R,4S,5S)-3,5-dihydroxy-2-phenoxy-tetrahydro-pyran-4-yl ester 
• 88087-54-1 Benzoic acid (3S,4R,5R,6S)-4,5-dihydroxy-6-phenoxy-tetrahydro-pyran-3-yl ester 
• 88087-62-1 C₂₅H₂₂O₇ 

Relevant articles and documents

Glycosylation reactions of 2,3,4-tri-O-chlorosulfonyl-β-L- fucopyranosyl chloride and 2,3,4-tri-O-chlorosulfonyl-β-D-xylopyranosyl chloride

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STEREOSPECIFICITY OF REACTIONS AT THE GLYCOSIDIC CENTER OF CARBOHYDRATES. IV. SYNTHESIS OF STEREOISOMERIC PHENYL ARABINOPYRANOSIDES

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