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Catalog Number:
16611
CAS Number:
70987-78-9
2 S -(+)-tosylate de glycidyle
Purity:
≥ 99 % (HPLC, pureté chirale)
Synonym(s):
( S -(+)-Oxirane-2-méthanol p -toluènesulfonate, ( S -(+)-Glycidyl p -toluènesulfonate
Hazmat
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Product Information

(2S)-(+)-Glycidyl tosylate is a versatile chemical compound widely utilized in organic synthesis and pharmaceutical applications. This compound, also known as glycidyl p-toluenesulfonate, serves as an effective electrophilic reagent, making it invaluable for the preparation of various functionalized compounds. Its unique epoxide structure allows for regioselective reactions, enabling researchers to create complex molecules with precision.

In the pharmaceutical industry, (2S)-(+)-Glycidyl tosylate is employed in the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs), facilitating the development of new therapeutic agents. Additionally, its reactivity with nucleophiles makes it a key player in the production of polymers and resins, enhancing material properties for industrial applications. The compound's ease of handling and stability under standard conditions further contribute to its appeal, making it a preferred choice for professionals seeking reliable and efficient reagents in their synthesis processes.

Synonyms
( S -(+)-Oxirane-2-méthanol p -toluènesulfonate, ( S -(+)-Glycidyl p -toluènesulfonate
CAS Number
70987-78-9
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C10H12O4S
Molecular Weight
228.26
MDL Number
MFCD00064489
PubChem ID
160868
Melting Point
45-48 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Optical Rotation
[a] D 20 = +18 ± 1º (C = 2,75 dans CHCl 3 )
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( S -(+)-Oxirane-2-méthanol p -toluènesulfonate, ( S -(+)-Glycidyl p -toluènesulfonate
CAS Number
70987-78-9
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C10H12O4S
Molecular Weight
228.26
MDL Number
MFCD00064489
PubChem ID
160868
Melting Point
45-48 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Optical Rotation
[a] D 20 = +18 ± 1º (C = 2,75 dans CHCl 3 )
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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

  • Synthetic Chemistry: This compound serves as a versatile building block in organic synthesis, particularly for creating complex molecules in pharmaceuticals and agrochemicals.
  • Drug Development: It is used in the synthesis of various drug candidates, enabling the development of new medications with improved efficacy and safety profiles.
  • Polymer Chemistry: The compound acts as a reactive monomer in the production of specialty polymers, enhancing material properties such as durability and chemical resistance.
  • Bioconjugation: It facilitates the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted therapies and diagnostic tools in biomedicine.
  • Research Applications: Researchers utilize it in studying reaction mechanisms and developing new synthetic methodologies, contributing to advancements in chemical science.

Citations