Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
45108
CAS Number:
158816-55-8
5-Éthynyl-1,2,3-trifluorobenzène
Purity:
≥ 98% (CG)
Synonym(s):
3,4,5-Trifluorophénylacétylène
Hazmat
Documents
$255.28 /1G
Taille
Request Bulk Quote
Product Information

5-Ethynyl-1,2,3-trifluorobenzene is a versatile compound known for its unique trifluoromethyl group, which enhances its reactivity and stability in various chemical reactions. This compound is particularly valuable in the field of organic synthesis, where it serves as an essential building block for the development of pharmaceuticals, agrochemicals, and advanced materials. Its ethynyl group allows for easy incorporation into larger molecular frameworks, making it a preferred choice for researchers looking to create complex structures with specific functionalities.

In addition to its synthetic applications, 5-Ethynyl-1,2,3-trifluorobenzene is also utilized in the development of fluorinated compounds, which are known for their unique properties such as increased lipophilicity and thermal stability. These characteristics make it an attractive option for industries focused on creating high-performance materials and specialty chemicals. With its ability to enhance molecular properties and facilitate innovative research, this compound stands out as a key player in modern chemical applications.

Synonyms
3,4,5-Trifluorophénylacétylène
CAS Number
158816-55-8
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 3 F 3
Molecular Weight
0
MDL Number
MFCD08458177
PubChem ID
22709071
Density
1.26
Appearance
Liquide transparent incolore à orange clair à jaune
Refractive Index
n20D 1,4720 - 1,4760
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
3,4,5-Trifluorophénylacétylène
CAS Number
158816-55-8
Purity
≥ 98% (CG)
Molecular Formula
C 8 H 3 F 3
Molecular Weight
0
MDL Number
MFCD08458177
PubChem ID
22709071
Density
1.26
Appearance
Liquide transparent incolore à orange clair à jaune
Refractive Index
n20D 1,4720 - 1,4760
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Ethynyl-1,2,3-trifluorobenzene is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, making it valuable for chemists developing new pharmaceuticals and agrochemicals.
  • Fluorinated Compounds: Its trifluoromethyl groups enhance the biological activity and stability of drugs, leading to improved efficacy in medicinal chemistry applications.
  • Material Science: Used in the development of advanced materials, such as polymers and coatings, due to its unique electronic properties, which can enhance material performance.
  • Research in Electronics: This compound is explored in the field of organic electronics, particularly in the fabrication of organic light-emitting diodes (OLEDs) and organic photovoltaics, contributing to energy-efficient technologies.
  • Analytical Chemistry: It acts as a reference standard in analytical methods, helping researchers ensure accuracy and reliability in the detection of fluorinated compounds in various samples.

Citations