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Catalog Number:
41381
CAS Number:
51800-98-7
(+)-3-(Trifluoroacetyl)camphor
Purity:
≥ 97.5% (GC)
Synonym(s):
3-(Trifluoroacetyl)-D-camphor
Hazmat
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Product Information

(+)-3-(Trifluoroacetyl)camphor is a versatile compound known for its unique trifluoroacetyl group, which enhances its reactivity and solubility in various organic solvents. This compound is particularly valuable in the field of organic synthesis, where it serves as an important intermediate for the preparation of various pharmaceuticals and agrochemicals. Its distinctive bicyclic structure contributes to its stability and effectiveness in chemical reactions, making it a preferred choice for researchers looking to develop new compounds with specific biological activities.

In addition to its applications in synthetic chemistry, (+)-3-(Trifluoroacetyl)camphor has been utilized in the formulation of fragrances and flavoring agents, capitalizing on its pleasant aroma and stability. Its ability to act as a chiral auxiliary also makes it a significant player in asymmetric synthesis, allowing chemists to produce enantiomerically pure compounds efficiently. With its broad range of applications, this compound is an essential tool for professionals in pharmaceuticals, agrochemicals, and fragrance industries, offering both practical benefits and innovative solutions.

Synonyms
3-(Trifluoroacetyl)-D-camphor
CAS Number
51800-98-7
Purity
≥ 97.5% (GC)
Molecular Formula
C12H15F3O2
Molecular Weight
0
MDL Number
MFCD00003746
PubChem ID
521351
Density
1.172 g/mL at 25 °C (Lit.)
Appearance
Colorless liquid
Boiling Point
100 - 101 °C / 16 mmHg (Lit.)
Refractive Index
n20D 1.451 (Lit.)
Optical Rotation
[α]20D = 142 - 154 ° (C = 2.3 in CH2Cl2)
Conditions
Store at RT
General Information
Synonyms
3-(Trifluoroacetyl)-D-camphor
CAS Number
51800-98-7
Purity
≥ 97.5% (GC)
Molecular Formula
C12H15F3O2
Molecular Weight
0
MDL Number
MFCD00003746
PubChem ID
521351
Density
1.172 g/mL at 25 °C (Lit.)
Appearance
Colorless liquid
Boiling Point
100 - 101 °C / 16 mmHg (Lit.)
Refractive Index
n20D 1.451 (Lit.)
Optical Rotation
[α]20D = 142 - 154 ° (C = 2.3 in CH2Cl2)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+)-3-(Trifluoroacetyl)camphor is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in creating compounds with enhanced biological activity.
  • Flavor and Fragrance Industry: Its unique scent profile makes it a valuable ingredient in the formulation of perfumes and flavorings, providing a fresh, camphoraceous note that is sought after in many products.
  • Analytical Chemistry: Used as a chiral selector in chromatography, it helps in the separation of enantiomers, which is crucial for the development of chiral drugs and ensuring their efficacy and safety.
  • Material Science: The compound is explored in the development of new materials, particularly in coatings and polymers, where its properties can enhance durability and resistance to environmental factors.
  • Research in Organic Synthesis: It acts as a reagent in various organic reactions, facilitating the formation of complex molecules and aiding researchers in the exploration of new synthetic pathways.

Citations