Structure

Phenyl 3,4,6-tri-O-acetyl-2-Deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-d-glucopyranoside

CAS
187022-49-7
Catalog Number
ACM187022497
Category
Other Products
Molecular Weight
572.84
Molecular Formula
C21H24Cl3NO9S

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Specification

Synonyms
187022-49-7, Phenyl 3,4,6-Tri-O-acetyl-2-deoxy-1-thio-2-(2,2,2-trichloroethoxyformamido)-beta-D-glucopyranoside, CTK8B3848, ANW-43300, P1866
IUPAC Name
[(2S,3S,4R,5S,6S)-3,4-diacetyloxy-6-phenylsulfanyl-5-(2,2,2-trichloroethoxycarbonylamino)oxan-2-yl]methyl acetate
SMILES
CC(=O)OCC1C(C(C(C(O1)SC2=CC=CC=C2)NC(=O)OCC(Cl)(Cl)Cl)OC(=O)C)OC(=O)C
InChI Key
AZDNCEYOFMNMSH-QTMHVTGLSA-N
Boiling Point
633.127ºC at 760 mmHg
Flash Point
336.703ºC
Density
1.457g/cm³
Exact Mass
571.02400
H-Bond Acceptor
10
H-Bond Donor
1

Upstream Synthesis Route 1

  • 108-98-5
  • 122210-01-9
  • 187022-49-7

Reference: [1] Chemical and Pharmaceutical Bulletin, 1997, vol. 45, # 2, p. 312 - 320
[2] Carbohydrate Research, 2017, vol. 452, p. 47 - 53
[3] Journal of Organic Chemistry, 2011, vol. 76, # 10, p. 3691 - 3709
[4] Angewandte Chemie - International Edition, 2014, vol. 53, # 31, p. 8190 - 8194[5] Angew. Chem., 2014, vol. 126, # 31, p. 8329 - 8333,5

Upstream Synthesis Route 2

  • 108-98-5
  • 187022-27-1
  • 187022-49-7

Reference: [1] Carbohydrate Research, 1996, vol. 295, p. 41 - 55

Upstream Synthesis Route 3

  • 136945-14-7
  • 675876-42-3
  • 187022-49-7
  • 676227-84-2

Reference: [1] Tetrahedron Letters, 2004, vol. 45, # 7, p. 1433 - 1436

Downstream Synthesis Route 1

  • 187022-49-7
  • 944060-21-3

Reference: [1]Synlett,2007,p. 818 - 820

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

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