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Catalog Number:
24478
CAS Number:
349-95-1
4-(Trifluoromethyl)benzyl alcohol
Purity:
≥ 99% (GC)
Synonym(s):
p-Trifluoromethylbenzyl alcohol
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Product Information

4-(Trifluoromethyl)benzyl alcohol is a versatile compound known for its unique trifluoromethyl group, which enhances its reactivity and solubility in various organic solvents. This compound is widely utilized in the synthesis of pharmaceuticals and agrochemicals, where the trifluoromethyl moiety can significantly improve the biological activity of the resulting products. Its ability to act as a building block in organic synthesis makes it invaluable for researchers looking to develop new compounds with enhanced properties.

In addition to its applications in drug discovery and development, 4-(Trifluoromethyl)benzyl alcohol is also employed in the production of specialty chemicals and materials. Its distinctive properties allow for the fine-tuning of chemical reactions, making it a preferred choice in the formulation of advanced materials and coatings. The compound's stability and reactivity profile provide researchers and industry professionals with a reliable tool for innovation in various fields, including medicinal chemistry and materials science.

Synonyms
p-Trifluoromethylbenzyl alcohol
CAS Number
349-95-1
Purity
≥ 99% (GC)
Molecular Formula
C8H7F3O
Molecular Weight
176.14
MDL Number
MFCD00004661
PubChem ID
67684
Melting Point
18-20 ?C
Density
1.286g/mL
Appearance
Colorless to light yellow liquid
Boiling Point
78-80 ?C
Refractive Index
(n20D) = 1.459
Conditions
Store at 0-8 °C
General Information
Synonyms
p-Trifluoromethylbenzyl alcohol
CAS Number
349-95-1
Purity
≥ 99% (GC)
Molecular Formula
C8H7F3O
Molecular Weight
176.14
MDL Number
MFCD00004661
PubChem ID
67684
Melting Point
18-20 ?C
Density
1.286g/mL
Appearance
Colorless to light yellow liquid
Boiling Point
78-80 ?C
Refractive Index
(n20D) = 1.459
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-(Trifluoromethyl)benzyl alcohol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders due to its unique trifluoromethyl group, which can enhance biological activity.
  • Organic Synthesis: It is commonly used in organic chemistry as a building block for creating more complex molecules, making it valuable for researchers developing new materials or compounds.
  • Fluorinated Compounds: The presence of the trifluoromethyl group allows for the production of fluorinated compounds, which are important in agrochemicals and specialty chemicals, providing enhanced stability and efficacy.
  • Material Science: This chemical is employed in the formulation of advanced materials, such as coatings and polymers, where its properties can improve durability and resistance to environmental factors.
  • Analytical Chemistry: It is used as a standard in analytical methods, helping researchers calibrate instruments and validate results in various chemical analyses.

Citations