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Catalog Number:
32381
CAS Number:
73346-74-4
-)-2,3- O -Isopropylidène-D-thréitol
Purity:
≥ 98% (CG)
Synonym(s):
(4 R ,5 R -2,2-diméthyl-1,3-dioxolane-4,5-diméthanol, (4 R ,5 R -(-)-4,5-bis(hydroxyméthyl)-2,2-diméthyl-1,3-dioxolane
Documents
$43.87 /1G
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
(4 R ,5 R -2,2-diméthyl-1,3-dioxolane-4,5-diméthanol, (4 R ,5 R -(-)-4,5-bis(hydroxyméthyl)-2,2-diméthyl-1,3-dioxolane
CAS Number
73346-74-4
Purity
≥ 98% (CG)
Molecular Formula
C7H14O4
Molecular Weight
162.19
MDL Number
MFCD00009761
PubChem ID
318275
Melting Point
47-52? C
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
88-90° C / 0,05 mmHg
Optical Rotation
[a]20/D= -3 à -5° (C=5 en acétone)
Conditions
Conserver à ≤ -10 °C
General Information
Synonyms
(4 R ,5 R -2,2-diméthyl-1,3-dioxolane-4,5-diméthanol, (4 R ,5 R -(-)-4,5-bis(hydroxyméthyl)-2,2-diméthyl-1,3-dioxolane
CAS Number
73346-74-4
Purity
≥ 98% (CG)
Molecular Formula
C7H14O4
Molecular Weight
162.19
MDL Number
MFCD00009761
PubChem ID
318275
Melting Point
47-52? C
Appearance
Poudre cristalline blanche à blanc cassé
Boiling Point
88-90° C / 0,05 mmHg
Optical Rotation
[a]20/D= -3 à -5° (C=5 en acétone)
Conditions
Conserver à ≤ -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(-)-2,3-O-Isopropylidene-D-threitol is widely utilized in research focused on:

  • Synthesis of Carbohydrate Derivatives: This compound serves as a key intermediate in the synthesis of various carbohydrate derivatives, which are essential in the development of pharmaceuticals and glycosylation reactions.
  • Protecting Group in Organic Chemistry: It acts as an effective protecting group for hydroxyl functionalities during multi-step organic synthesis, enhancing the yield and purity of final products.
  • Research in Glycobiology: The compound is valuable in glycobiology studies, aiding in the exploration of glycan structures and their biological functions, which can lead to advancements in drug development.
  • Development of Antiviral Agents: Its derivatives have shown potential in the formulation of antiviral agents, contributing to the fight against viral infections by modifying sugar moieties.
  • Biochemical Applications: Used in the preparation of various biochemical probes, it helps researchers study enzyme activities and interactions, providing insights into metabolic pathways.

Citations