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Structure

Allyl alpha-D-glucopyranoside

CAS
7464-56-4
Catalog Number
ACM7464564
Category
Other Products
Molecular Weight
220.22
Molecular Formula
C9H16O6

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Specification

Synonyms
1-O-allyl-glucopyranoside; ALLYL A-D-GLUCOPYRANOSIDE;
IUPAC Name
2-(hydroxymethyl)-6-prop-2-enoxyoxane-3,4,5-triol
InChI Key
XJNKZTHFPGIJNS-UHFFFAOYSA-N
Boiling Point
415ºC at 760 mmHg
Melting Point
138-141ºC
Flash Point
204.8ºC
Density
1.37 g/cm³
Appearance
white powder
Exact Mass
220.09500
H-Bond Acceptor
6
H-Bond Donor
4

Upstream Synthesis Route 1

  • 50-99-7
  • 107-18-6
  • 7464-56-4

Reference: [1]Location in patent: scheme or table
Hassan, Hammed H.A.M.
[Letters in Organic Chemistry, 2010, vol. 7, # 2, p. 127 - 135]
[2]Talley et al.
[Journal of the American Chemical Society, 1945, vol. 67, p. 2037]
Danielli et al.
[Biochemical Journal, 1947, vol. 41, p. 325,332]
[3]Hetfleisch-Stephan; Schunk; Rudiger
[Pharmazie, 1994, vol. 49, # 2-3, p. 125 - 130]
[4]Koto, Shinkiti; Shinoda, Yoshika; Hirooka, Motoko; Sekino, Akiko; Ishizumi, Sachiko; Koma, Mutsuko; Matuura, Chieko; Sakata, Naoko
[Bulletin of the Chemical Society of Japan, 2003, vol. 76, # 8, p. 1603 - 1615]

Upstream Synthesis Route 2

  • 2280-44-6
  • 107-18-6
  • 7464-56-4

Reference: [1]Schindler, Corinna S.; Bertschi, Louis; Carreira, Erick M.
[Angewandte Chemie - International Edition, 2010, vol. 49, # 48, p. 9229 - 9232]

Downstream Synthesis Route 1

  • 106-95-6
  • 7464-56-4
  • 185564-68-5

Reference: [1]Location in patent: experimental part
Hassan, Hammed H.A.M.
[Letters in Organic Chemistry, 2010, vol. 7, # 2, p. 127 - 135]
[2]Talley et al.
[Journal of the American Chemical Society, 1945, vol. 67, p. 2037]

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

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