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Catalog Number:
32204
CAS Number:
195976-07-9
Ester tert -butylique de O-(2-azido-4,6- O -benzylidène-2-désoxy-α-D-galactopyranosyl) -N -[( 9H- fluorén-9-ylméthoxy)carbonyl]-L-thréonine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester tert -butylique de O-(2-azido-4,6- O -benzylidène-2-désoxy-α-D-galactopyranosyl) -N -Fmoc-L-thréonine, Fmoc-Thr[GalN3[46Bzd]-α]-OtBu
Documents
$325.09 /5 mg
Taille
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Product Information

Conserver à l'abri des agents oxydants, des sources d'ignition. Conserver sous gaz inerte (par exemple Argon).

Synonyms
Ester tert -butylique de O-(2-azido-4,6- O -benzylidène-2-désoxy-α-D-galactopyranosyl) -N -Fmoc-L-thréonine, Fmoc-Thr[GalN3[46Bzd]-α]-OtBu
CAS Number
195976-07-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C36H40N4O9
Molecular Weight
672.74
MDL Number
MFCD11112165
PubChem ID
76030746
Appearance
Poudre cristalline jaune clair à jaune
Optical Rotation
[a]20/D= +111 à +117° (C=1 dans CHCl 3 )
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
Ester tert -butylique de O-(2-azido-4,6- O -benzylidène-2-désoxy-α-D-galactopyranosyl) -N -Fmoc-L-thréonine, Fmoc-Thr[GalN3[46Bzd]-α]-OtBu
CAS Number
195976-07-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C36H40N4O9
Molecular Weight
672.74
MDL Number
MFCD11112165
PubChem ID
76030746
Appearance
Poudre cristalline jaune clair à jaune
Optical Rotation
[a]20/D= +111 à +117° (C=1 dans CHCl 3 )
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

O-(2-Azido-4,6-O-benzylidene-2-deoxy-a-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-th is widely utilized in research focused on:

  • Drug Development: This compound serves as a versatile intermediate in the synthesis of glycosylated drugs, enhancing their efficacy and targeting capabilities.
  • Bioconjugation: Its azido group allows for click chemistry applications, facilitating the attachment of biomolecules for targeted drug delivery systems.
  • Glycobiology Studies: Researchers use this compound to investigate carbohydrate-protein interactions, aiding in the understanding of cellular processes and disease mechanisms.
  • Diagnostic Applications: It can be employed in the development of diagnostic agents that utilize glycan recognition, improving the specificity of disease detection methods.
  • Material Science: The compound is explored for creating functionalized materials with specific properties, such as enhanced biocompatibility for biomedical applications.

Citations