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Catalog Number:
37523
CAS Number:
340-06-7
(S-(+)-α-(Trifluoromethyl)benzyl alcohol
Purity:
≥ 98% (GC)
Synonym(s):
(+)-Phenyl(trifluoromethyl)carbinol, (S-(+)-1-Phenyl-2,2,2-trifluoroethanol
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$356.03 /1G
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Product Information

(S)-(+)-a-(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 particularly valuable in the pharmaceutical and agrochemical industries, where it serves as a key intermediate in the synthesis of biologically active molecules. Its ability to modify the electronic properties of aromatic compounds makes it an essential building block for researchers looking to develop new drugs or crop protection agents.

In addition to its applications in synthesis, (S)-(+)-a-(Trifluoromethyl)benzyl alcohol is also utilized in the production of specialty chemicals and materials, where its distinct properties can improve product performance. Its chirality offers potential advantages in asymmetric synthesis, making it a preferred choice for chemists aiming to create enantiomerically pure compounds. With its broad range of applications and unique characteristics, this compound is an excellent addition to any research or industrial setting focused on innovation and efficiency.

Synonyms
(+)-Phenyl(trifluoromethyl)carbinol, (S-(+)-1-Phenyl-2,2,2-trifluoroethanol
CAS Number
340-06-7
Purity
≥ 98% (GC)
Molecular Formula
C8H7F3O
Molecular Weight
176.14
MDL Number
MFCD00077845
PubChem ID
95556
Density
1.3
Appearance
Colorless to Light yellow clear liquid
Boiling Point
127 °C
Refractive Index
1.46
Optical Rotation
[α]20D = 30 - 33 ° (neat)
Conditions
Store at RT
General Information
Synonyms
(+)-Phenyl(trifluoromethyl)carbinol, (S-(+)-1-Phenyl-2,2,2-trifluoroethanol
CAS Number
340-06-7
Purity
≥ 98% (GC)
Molecular Formula
C8H7F3O
Molecular Weight
176.14
MDL Number
MFCD00077845
PubChem ID
95556
Density
1.3
Appearance
Colorless to Light yellow clear liquid
Boiling Point
127 °C
Refractive Index
1.46
Optical Rotation
[α]20D = 30 - 33 ° (neat)
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-(+)-a-(Trifluoromethyl)benzyl alcohol is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific biological pathways due to its unique trifluoromethyl group, enhancing bioactivity.
  • Material Science: It is used in the formulation of advanced materials, including coatings and polymers, where its properties contribute to improved chemical resistance and thermal stability.
  • Organic Synthesis: The compound is a valuable building block in organic chemistry, facilitating the creation of complex molecules with high precision, which is essential for researchers developing new compounds.
  • Agricultural Chemicals: It finds applications in the production of agrochemicals, where its ability to enhance the efficacy of active ingredients leads to more effective pest control solutions.
  • Fluorinated Compounds Research: This chemical is instrumental in studies focused on fluorinated compounds, providing insights into their behavior and applications, which are crucial in various industrial processes.

Citations