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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
Documents
$84.83 /1G
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Product 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
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!
-
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