3365-67-1 Usage
Uses
Used in Polymer Production:
Hexacosanedioic acid is utilized as a key component in the synthesis of polymers, specifically for the manufacturing of nylon and polyurethane. Its role in these applications is crucial for creating high-performance materials with desirable properties.
Used in Pharmaceutical Industry:
Within the pharmaceutical sector, hexacosanedioic acid is employed for its potential applications, although the specific uses are not detailed in the provided materials. Its inclusion in this industry suggests that it may have roles in drug formulation or as an intermediate in the synthesis of pharmaceutical compounds.
Used in Cosmetics Industry:
In the cosmetics industry, hexacosanedioic acid is used for its potential applications, which might include its use in the formulation of various cosmetic products, although the exact reasons are not specified in the materials.
Used as a Corrosion Inhibitor:
Hexacosanedioic acid has been investigated for its potential as a corrosion inhibitor. This application type is valuable for protecting materials from degradation in various industrial settings.
Used in Lubricants:
As a component in lubricants, hexacosanedioic acid contributes to the enhancement of the performance characteristics of these products, although the specific reasons for its use in this context are not elaborated upon in the provided materials.
Check Digit Verification of cas no
The CAS Registry Mumber 3365-67-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3365-67:
(6*3)+(5*3)+(4*6)+(3*5)+(2*6)+(1*7)=91
91 % 10 = 1
So 3365-67-1 is a valid CAS Registry Number.
3365-67-1Relevant academic research and scientific papers
INTRAMOLECULAR END-TO-END REACTIONS OF PHOTOACTIVE TERMINAL GROUPS LINKED BY POLYMETHYLENE CHAINS.
Ashikaga,Ito,Yamamoto,Nishijima
, p. 198 - 204 (2007/10/02)
Intramolecular end-to-end reactions of a pair of photoactive terminal groups, dibenz left bracket b,f right bracket azepine (DBA) chromophores, linked by a series of polymethylene chains (DBA-CO(CH//2)//nCO-DBA, n equals 2-30) were studied by two different approaches. One approach is to measure the intramolecular deactivation rate constants of the excited triplet state of terminal DBA groups by the nanosecond laser photolysis and the other is to measure the intramolecular photocyclization rates of these bichromophoric compounds by the quantitative product analysis with GPC. The excited triplet state of the DBA group is the intermediate of the reaction.
