2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide

• CAS: 572-09-8
• Catalog Number: ACM572098
• Category: Other Products
• Molecular Weight: 411.2
• Molecular Formula: C14H19BrO9
• Synonyms: Acetobromo-α-D-glucose;Acetobromglucose;Tetraacetyl bromoglucose
• IUPAC Name: [(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-bromooxan-2-yl]methyl acetate
• SMILES: CC(=O)OC[C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)Br)OC(=O)C)OC(=O)C)OC(=O)C
• InChI: InChI=1S/C14H19BrO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1
• InChI Key: CYAYKKUWALRRPA-RGDJUOJXSA-N
• Boiling Point: 412ºC at 760 mmHg
• Melting Point: 86-89 °C
• Density: 1.49±0.1 g/ml
• Appearance: White to beige powder
• EC Number: 209-339-0
• Exact Mass: 410.02100
• Hazard Statements: Xi
• H-Bond Acceptor: 9
• H-Bond Donor: 0
• Safety Description: S24/25
• Solubility In Water: Decomposes
• Stability: Stable. Combustible. Incompatible with strong oxidizing agents.

Synthetic Use

Downstream Synthesis Route 1

• 773-76-2
• 572-09-8

• 492-61-5
• 130-16-5

Reference: [1] Dalton Transactions, 2013, vol. 42, # 6, p. 2023 - 2034

Downstream Synthesis Route 2

• 446-72-0
• 572-09-8

• 529-59-9

Reference: [1] Journal of the Chemical Society - Perkin Transactions 1, 1998, # 16, p. 2481 - 2484

Downstream Synthesis Route 3

• 572-09-8

• 10338-51-9

Reference: [1] Phytochemistry, 1988, vol. 27, # 6, p. 1813 - 1816
[2] Tetrahedron, 1989, vol. 45, # 12, p. 3673 - 3682

Downstream Synthesis Route 4

• 2150-45-0
• 572-09-8

• 116865-53-3

Reference: [1]Justus Liebigs Annalen der Chemie,1938,vol. 533,p. 278,286

Downstream Synthesis Route 5

• 94-26-8
• 572-09-8

• 121970-17-0

Reference: [1]Archiv der Pharmazie,1959,vol. 292,p. 341,346

* For details of the synthesis route, please refer to the original source to ensure accuracy.