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Catalog Number:
16518
CAS Number:
113826-06-5
2 R -(-)-Tosilato de glicidilo
Purity:
≥ 99% (HPLC, pureza quiral)
Synonym(s):
( R -(-)-P-toluenosulfonato de oxirano-2-metanol, ( R -(-)-P-toluenosulfonato de glicidilo
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Product Information

(2R)-(-)-Glycidyl tosylate is a versatile compound widely recognized for its utility in organic synthesis and pharmaceutical applications. This chiral epoxide serves as an effective electrophile, facilitating nucleophilic substitutions that are crucial in the development of various chemical entities. Its unique structure allows for regioselective reactions, making it an invaluable tool for researchers aiming to create complex molecules with precision. The compound is particularly beneficial in the synthesis of glycosides, amino acids, and other biologically active compounds, enhancing the efficiency of synthetic pathways in medicinal chemistry.

In addition to its synthetic applications, (2R)-(-)-Glycidyl tosylate is also employed in the production of polymeric materials, where it contributes to the development of advanced materials with tailored properties. Its ability to undergo ring-opening reactions makes it suitable for creating functionalized polymers that can be utilized in coatings, adhesives, and sealants. With its broad range of applications and the ability to facilitate complex chemical transformations, (2R)-(-)-Glycidyl tosylate stands out as a key reagent for professionals in the fields of chemistry and materials science.

Synonyms
( R -(-)-P-toluenosulfonato de oxirano-2-metanol, ( R -(-)-P-toluenosulfonato de glicidilo
CAS Number
113826-06-5
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C10H12O4S
Molecular Weight
228.26
MDL Number
MFCD00010834
PubChem ID
160868
Melting Point
45-48 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -18 ± 1º (C=2,75 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
( R -(-)-P-toluenosulfonato de oxirano-2-metanol, ( R -(-)-P-toluenosulfonato de glicidilo
CAS Number
113826-06-5
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C10H12O4S
Molecular Weight
228.26
MDL Number
MFCD00010834
PubChem ID
160868
Melting Point
45-48 ?C
Appearance
Polvo cristalino de color blanco a blanquecino.
Optical Rotation
[a] D 20 = -18 ± 1º (C=2,75 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2R)-(-)-Glycidyl tosylate is widely utilized in research focused on

  • Synthetic Chemistry: This compound serves as a versatile building block in organic synthesis, enabling the formation of various complex molecules through nucleophilic substitution reactions.
  • Pharmaceutical Development: It is employed in the synthesis of pharmaceutical intermediates, allowing researchers to create new drugs with improved efficacy and reduced side effects.
  • Polymer Chemistry: The compound is used to modify polymer properties, enhancing their performance in applications such as coatings, adhesives, and sealants.
  • Bioconjugation: It facilitates the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems and diagnostic tools.
  • Material Science: The chemical is applied in the development of functional materials, contributing to advancements in electronics and nanotechnology through its unique reactivity.

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