115224-00-5 Usage
Description
3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR is a chemical compound derived from camphor, a natural monoterpene ketone found in the wood of the camphor laurel tree. 3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR is characterized by the presence of a heptafluorobutyryl group, which imparts unique properties to the molecule. It is known for its potential applications in various fields due to its distinct chemical structure and reactivity.
Uses
Used in Catalyst Preparation:
3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR is used as a precursor in the preparation of mesoporous metal-organic hybrid materials. These materials are utilized as catalysts in the asymmetric hetero-Diels-Alder cyclization of Danishefsky's diene with benzaldehydes. The heptafluorobutyryl group in the compound enhances the catalytic activity and selectivity of the resulting materials.
Used in Chiral Complex Synthesis:
In the field of coordination chemistry, 3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR serves as a precursor in the synthesis of chiral tetrakis(β-diketonate) Ln(III) complexes. These complexes are of significant interest due to their potential applications in asymmetric catalysis, molecular recognition, and as chiral dopants in various materials. The heptafluorobutyryl group in the compound plays a crucial role in the formation of the desired chiral complexes, contributing to their unique properties and reactivity.
Used in Chemical Synthesis:
3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR can also be employed as an intermediate in the synthesis of various organic compounds, particularly those requiring a fluorinated moiety. The presence of the heptafluorobutyryl group allows for further functionalization and modification of the molecule, enabling the development of new compounds with tailored properties for specific applications.
Used in Pharmaceutical Industry:
Due to its unique chemical structure, 3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR may have potential applications in the pharmaceutical industry as a building block for the development of new drugs. The heptafluorobutyryl group could impart specific pharmacological properties to the resulting drug candidates, such as improved lipophilicity, enhanced bioavailability, or targeted delivery to specific tissues or organs.
Used in Material Science:
In the field of material science, 3-(HEPTAFLUOROBUTYRYL)-I-CAMPHOR could be used to develop novel materials with unique properties. The heptafluorobutyryl group may contribute to the formation of materials with enhanced thermal stability, chemical resistance, or specific optical and electronic properties, making them suitable for various applications, such as in coatings, adhesives, or sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 115224-00-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,2 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115224-00:
(8*1)+(7*1)+(6*5)+(5*2)+(4*2)+(3*4)+(2*0)+(1*0)=75
75 % 10 = 5
So 115224-00-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H15F7O2/c1-10(2)6-4-5-11(10,3)8(22)7(6)9(23)12(15,16)13(17,18)14(19,20)21/h6-7H,4-5H2,1-3H3/t6-,7?,11+/m0/s1
115224-00-5Relevant articles and documents
Synthesis of chiral 1,3-diketones from the coupling reaction of (+)-3 α-bromocamphor with acyl chlorides in the presence of samarium diiodide
Wei, Han-Xun,Wang, Zhi-Min,Shi, Min
, p. 909 - 910 (1999)
Some hindered chiral 1,3-diketones were successfully synthesized from the reaction of (+)-3α-bromocamphor with acyl chlorides in the presence of samarium diiodide (SmI2) under mild reaction conditions in high yields.
