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Catalog Number:
24595
CAS Number:
2627-86-3
(S)-(-)-alpha-méthylbenzylamine
Purity:
≥ 98,5 % (pureté chirale)
Synonym(s):
(S)-(-)-1-phényléthylamine
Hazmat
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Informations sur le produit

(S)-(-)-alpha-Methylbenzylamine is a versatile chiral amine widely utilized in the synthesis of pharmaceuticals and agrochemicals. This compound is recognized for its ability to act as a building block in the production of various biologically active molecules, including antidepressants and anti-inflammatory agents. Its unique stereochemistry enhances its effectiveness in asymmetric synthesis, making it a valuable asset in the development of enantiomerically pure compounds. Researchers appreciate its role in catalyzing reactions that require specific chirality, thereby improving the efficacy and safety profiles of the resulting products.

In addition to its pharmaceutical applications, (S)-(-)-alpha-Methylbenzylamine is also employed in the synthesis of specialty chemicals and as a reagent in organic chemistry. Its favorable properties, such as high reactivity and selectivity, position it as a preferred choice for professionals seeking reliable and efficient solutions in their chemical processes. With its proven track record in enhancing product performance, this compound is essential for those aiming to innovate in their respective fields.

Numéro CAS 
2627-86-3
Formule moléculaire
C8H11N
Poids moléculaire 
121.18
Rotation optique 
[a] = -39 ± 2º (pur)
Informations générales
Numéro CAS 
2627-86-3
Formule moléculaire
C8H11N
Poids moléculaire 
121.18
Rotation optique 
[a] = -39 ± 2º (pur)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
-
Applications

(S)-(-)-alpha-Methylbenzylamine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in the production of chiral amines, which are crucial for creating effective drug formulations.
  • Asymmetric Synthesis: It plays a key role in asymmetric synthesis processes, allowing chemists to produce compounds with specific configurations that are often more biologically active, enhancing the efficacy of drugs.
  • Analytical Chemistry: Used as a chiral derivatizing agent in analytical methods, it helps in the separation and identification of enantiomers, which is vital for quality control in drug manufacturing.
  • Agrochemical Applications: The compound is also explored in the formulation of agrochemicals, where its properties can improve the effectiveness of pesticides and herbicides, contributing to more sustainable agricultural practices.
  • Material Science: In the field of material science, it is utilized in the development of new polymers and coatings, enhancing their properties such as adhesion and durability.

Citations