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Catalog Number:
41498
CAS Number:
154727-51-2
( S )-2-(Trifluorometil)piperidina
Purity:
≥ 96,5 % (GC)
Hazmat
Documents
$48.27 /250 mg
Tamaño
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Product Information

(S)-2-(Trifluoromethyl)piperidine is a versatile compound recognized for its unique trifluoromethyl group, which enhances its chemical reactivity and stability. This compound is particularly valuable in the pharmaceutical and agrochemical industries, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its distinct properties make it an ideal candidate for developing novel therapeutic agents and crop protection products. Researchers appreciate its ability to modify the pharmacokinetic profiles of drug candidates, potentially leading to improved efficacy and reduced side effects.

In addition to its applications in drug development, (S)-2-(Trifluoromethyl)piperidine is also utilized in the synthesis of advanced materials and specialty chemicals. Its trifluoromethyl group imparts unique electronic properties, making it a valuable building block for creating compounds with enhanced performance characteristics. This compound's ability to facilitate the development of innovative solutions in diverse fields underscores its importance to researchers and industry professionals alike.

CAS Number
154727-51-2
Purity
≥ 96,5 % (GC)
Molecular Formula
C6H10F3N
Molecular Weight
153.15
MDL Number
MFCD11226597
PubChem ID
11263608
Density
1,161 g/mL a 25 °C
Appearance
Líquido incoloro a amarillo a marrón.
Boiling Point
72 °C (Literatura)
Refractive Index
n20D 1,39
Optical Rotation
[ á]22/D = -14,4 ° (C = 0,5 en metanol)
Conditions
Tienda en RT
General Information
CAS Number
154727-51-2
Purity
≥ 96,5 % (GC)
Molecular Formula
C6H10F3N
Molecular Weight
153.15
MDL Number
MFCD11226597
PubChem ID
11263608
Density
1,161 g/mL a 25 °C
Appearance
Líquido incoloro a amarillo a marrón.
Boiling Point
72 °C (Literatura)
Refractive Index
n20D 1,39
Optical Rotation
[ á]22/D = -14,4 ° (C = 0,5 en metanol)
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-2-(Trifluoromethyl)piperidine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders due to its ability to modulate neurotransmitter systems.
  • Agrochemical Formulations: It is used in the formulation of agrochemicals, enhancing the efficacy of pesticides and herbicides by improving their stability and bioavailability in agricultural applications.
  • Material Science: The compound is employed in the creation of advanced materials, including polymers and coatings, where its unique trifluoromethyl group contributes to improved chemical resistance and durability.
  • Research in Organic Chemistry: It acts as a valuable building block in organic synthesis, allowing researchers to create complex molecules with specific properties, which is essential for innovation in chemical research.
  • Fluorine Chemistry: This chemical plays a significant role in fluorine chemistry, where it is used to study the effects of fluorination on molecular properties, aiding in the design of new compounds with desirable characteristics.

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