110906-68-8

Basic information

• Product Name: C₂₈H₃₆O₇
• CAS NO: 110906-68-8
• Molecular Weight: 484.59
• Mol File: 110906-68-8.mol

Chemical Properties

• CAS DataBase Reference: C₂₈H₃₆O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₈H₃₆O₇(110906-68-8)
• EPA Substance Registry System: C₂₈H₃₆O₇(110906-68-8)

Safety Data

• Hazardous Substances Data: 110906-68-8(Hazardous Substances Data)

Upstream product

• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 110906-70-2 Benzoic acid (2R,3R,4R,6S)-3-((2R,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-methyl-3-phenylselanyl-tetrahydro-pyran-2-yloxy)-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-yl ester 
• 110906-66-6 Benzoic acid (2R,3R,4R,6S)-4-((2R,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-methyl-3-phenylselanyl-tetrahydro-pyran-2-yloxy)-6-methoxy-2,4-dimethyl-tetrahydro-pyran-3-yl ester 
• 110906-71-3 (2R,3R,4R,6S)-3-((2R,3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-methyl-3-phenylselanyl-tetrahydro-pyran-2-yloxy)-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-ol 
• 110906-65-5 (2R,3R,4R,6S)-4-((2R,3S,4S,5R,6R)-4,5-Bis-benzyloxy-6-methyl-3-phenylselanyl-tetrahydro-pyran-2-yloxy)-6-methoxy-2,4-dimethyl-tetrahydro-pyran-3-ol 
• 72244-36-1 (2R,4aR,6S,8aS)-6-Methoxy-8-methylene-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 63598-31-2 methyl 4,6-O-(R)-benzylidene-2-deoxy-α-D-erythrohexopyranosid-3-ulose 
• 73712-09-1 methyl 2,6-dideoxy-3-C-methyl-α-D-arabino-hexopyranoside 
• 110906-72-4 C₃₄H₄₂O₈Se 
• 110906-67-7 C₃₄H₄₂O₈Se 
• 110906-64-4 Benzoic acid (2R,3R,4R,6S)-3-hydroxy-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-yl ester 
• 78086-61-0 (2R,3S,4R)-2-Methyl-3,4-dihydro-2H-pyran-3,4-diol 
• 111002-90-5 1,5-anhydro-3,4-di-O-benzyl-2,6-dideoxy-D-arabino-hex-1-enitol 
• 100-39-0 benzyl bromide 

Downstream Products

• 110906-73-5 (3R,4R,5R)-3,4-Bis-benzyloxy-5-hydroxy-hexanoic acid (2R,3R,4R,6S)-4-hydroxy-6-methoxy-2,4-dimethyl-tetrahydro-pyran-3-yl ester 
• 110906-74-6 (3R,4R,5R)-3,4-Bis-benzyloxy-5-hydroxy-hexanoic acid (2R,3R,4R,6S)-3-hydroxy-6-methoxy-2,4-dimethyl-tetrahydro-pyran-4-yl ester 

Relevant articles and documents

SYNTHESIS OF THE DISACCHARIDE C-D FRAGMENT FOUND IN EVERNINOMICIN-C AND -D, AVALAMYCIN-A AND -C, AND CURAMYCIN-A: STEREOCHEMISTRY AT THE SPIRO-ORTHOLACTONE CENTER

The two isomers at the spiro-ortholactone center of the disaccharide C-D fragment of orthosomycins have been synthesized.Their mild acidic hydrolysis was under stereoelectronic control with each isomer leading to only one ester.It is therefore possible, f