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Catalog Number:
32363
CAS Number:
934591-76-1
5-acétamido-7,8,9-tri- O -acétyl-5- N ,4- O -carbonyl-3,5-didésoxy-2- S -phényl-2-thio-D-glycéro-β-D-galacto-2-nonulopyranosylonate de méthyle
Purity:
≥ 98 % (ELSD)
Synonym(s):
(Phényl5-acétamido-7,8,9-tri- O -acétyl-5- N ,4- O -carbonyl-3,5-didésoxy-2-thio-D-glycéro-β-D-galacto-2-nonulopyranoside)onate de méthyle
Documents
$106.96 /25 mg
Taille
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Product Information

Conserver à l'abri des agents oxydants forts, des sources d'inflammation.

Synonyms
(Phényl5-acétamido-7,8,9-tri- O -acétyl-5- N ,4- O -carbonyl-3,5-didésoxy-2-thio-D-glycéro-β-D-galacto-2-nonulopyranoside)onate de méthyle
CAS Number
934591-76-1
Purity
≥ 98 % (ELSD)
Molecular Formula
C 25 H 29 NON 12 S
Molecular Weight
567.56
MDL Number
MFCD22581442
PubChem ID
102340779
Melting Point
150 - 154 °C
Appearance
Poudre blanche à marron clair
Optical Rotation
[a] 20 D = -120 à -126° (C=0,8 dans CHCl3)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
(Phényl5-acétamido-7,8,9-tri- O -acétyl-5- N ,4- O -carbonyl-3,5-didésoxy-2-thio-D-glycéro-β-D-galacto-2-nonulopyranoside)onate de méthyle
CAS Number
934591-76-1
Purity
≥ 98 % (ELSD)
Molecular Formula
C 25 H 29 NON 12 S
Molecular Weight
567.56
MDL Number
MFCD22581442
PubChem ID
102340779
Melting Point
150 - 154 °C
Appearance
Poudre blanche à marron clair
Optical Rotation
[a] 20 D = -120 à -126° (C=0,8 dans CHCl3)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Methyl 5-acetamido-7,8,9-tri-O-acetyl-5-N,4-O-carbonyl-3,5-dideoxy-2-S-phenyl-2-thio-D-glycero-b-D-g is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in synthesizing various pharmaceuticals, particularly those targeting metabolic disorders.
  • Biochemical Research: It is employed in studies related to enzyme inhibition and protein interactions, aiding researchers in understanding complex biological processes.
  • Drug Formulation: The compound's unique properties make it suitable for formulating drug delivery systems, enhancing the bioavailability of active ingredients.
  • Analytical Chemistry: Used as a standard in chromatography, it helps in the accurate quantification of similar compounds in complex mixtures.
  • Cosmetic Industry: Its application extends to cosmetic formulations, where it acts as a stabilizing agent, improving the shelf-life and effectiveness of products.

Citations