Structure

b-D-Glucopyranose,1,2,3,4-tetraacetate

CAS
13100-46-4
Catalog Number
ACM13100464
Category
Other Products
Molecular Weight
348.3026
Molecular Formula
C14H20O10

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  • Product Description
  • Case Study
  • Custom Reviews
  • Custom Q&A
  • Synthetic Use
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Specification

Synonyms
390879_ALDRICH, MolPort-001-780-270, CID349482, NSC409250, 1,2,3,4-Tetra-O-acetyl-beta-D-glucopyranose, 13100-46-4
IUPAC Name
[4,5,6-triacetyloxy-2-(hydroxymethyl)oxan-3-yl] acetate
SMILES
CC(=O)OC1C(OC(C(C1OC(=O)C)OC(=O)C)OC(=O)C)CO
InChI Key
FEQXFAYSNRWXDW-UHFFFAOYSA-N
Boiling Point
418.4ºC at 760 mmHg
Melting Point
126-128ºC(lit.)
Flash Point
145.6ºC
Density
1.33 g/cm³
EC Number
236-018-2
Exact Mass
348.10600
Hazard Statements
Xi
H-Bond Acceptor
10
H-Bond Donor
1

Upstream Synthesis Route 1

  • 37074-90-1
  • 13100-46-4

Reference: [1]Padyukova, N. Sh.; Afsar, S.; Dixon, H. B. F.; Karpeiskii, M. Ya.
[Russian Journal of Bioorganic Chemistry, 1995, vol. 21, # 5, p. 328 - 331][Bioorganicheskaya Khimiya, 1995, vol. 21, # 5, p. 382 - 385]

Downstream Synthesis Route 1

  • 13100-46-4
  • 32449-92-6

Reference: [1] Journal of the Chemical Society, 1939, p. 1529

Downstream Synthesis Route 2

  • 14227-66-8
  • 13100-46-4
  • 55287-00-8

Reference: [1]Helvetica Chimica Acta,1984,vol. 67,p. 378 - 385
[2]Justus Liebigs Annalen der Chemie,1926,vol. 450,p. 229,236

Downstream Synthesis Route 3

  • 2524-64-3
  • 13100-46-4
  • 108321-48-8

Reference: [1]Location in patent: experimental part
Golicnik, Marko; Olguin, Luis F.; Feng, Guoqiang; Baxter, Nicola J.; Waltho, Jonathan P.; et al.
[Journal of the American Chemical Society, 2009, vol. 131, p. 1575 - 1588]
[2]Lardy; Fischer
[Journal of Biological Chemistry, 1946, vol. 164, p. 513,516, 517][Biochemical Preparations, 1952, vol. 2, p. 39,41]

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

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